rs_ID |
Location |
Functional Annotation |
rs2545167 |
Chr5:112213071(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs580237 |
Chr5:112194032(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |
rs368575 |
Chr5:112204896(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs818425 |
Chr5:112226655(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs460832 |
Chr5:112225148(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs430665 |
Chr5:112228667(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant |
rs712665 |
Chr5:112227799(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; missense_variant; nc_transcript_variant; non_coding_exon_variant |
rs465454 |
Chr5:112230331(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs519397 |
Chr5:112229688(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs461866 |
Chr5:112231450(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs455412 |
Chr5:112224389(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs456313 |
Chr5:112224952(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs712662 |
Chr5:112222694(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs458451 |
Chr5:112224331(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1069061 |
Chr5:112218982(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs818427 |
Chr5:112221869(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs1093611 |
Chr5:112218476(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs1093677 |
Chr5:112218700(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs2545166 |
Chr5:112213805(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant; non_coding_exon_variant |
rs419632 |
Chr5:112216389(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs382260 |
Chr5:112210344(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs9011 |
Chr5:112212608(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs463229 |
Chr5:112201284(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs7213 |
Chr5:112203564(Fwd) |
3_prime_UTR_variant; NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs351769 |
Chr5:112199974(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs495794 |
Chr5:112201094(Fwd) |
NMD_transcript_variant; downstream_gene_variant; intron_variant; nc_transcript_variant |
rs351770 |
Chr5:112199199(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs372492 |
Chr5:112198015(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs431287 |
Chr5:112197986(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs712668 |
Chr5:112197637(Fwd) |
NMD_transcript_variant; intron_variant; nc_transcript_variant; upstream_gene_variant |
rs429427 |
Chr5:112194693(Fwd) |
NMD_transcript_variant; intron_variant; upstream_gene_variant |