rs_ID |
Location |
Functional Annotation |
rs11133792 |
chr5:1477231(Fwd) |
downstream_gene_variant; intron_variant; NMD_transcript_variant |
rs12654851 |
chr5:1454004(Fwd) |
downstream_gene_variant |
rs11750173 |
chr5:1460131(Fwd) |
downstream_gene_variant; intron_variant; NMD_transcript_variant |
rs2292023 |
chr5:1461389(Fwd) |
3_prime_UTR_variant; downstream_gene_variant; NMD_transcript_variant |
rs9728 |
chr5:1462098(Fwd) |
3_prime_UTR_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant |
rs2277006 |
chr5:1466919(Fwd) |
nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; synonymous_variant |
rs4608970 |
chr5:1519197(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2963282 |
chr5:1512208(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2962041 |
chr5:1511222(Fwd) |
intron_variant; nc_transcript_variant; NMD_transcript_variant |
rs2078247 |
chr5:1452280(Fwd) |
downstream_gene_variant |
rs17588991 |
chr5:1501695(Fwd) |
nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant; synonymous_variant |
rs8352 |
chr5:1463051(Fwd) |
3_prime_UTR_variant; nc_transcript_variant; NMD_transcript_variant; non_coding_exon_variant |
rs27052 |
chr5:1470069(Fwd) |
intron_variant; NMD_transcript_variant; upstream_gene_variant |
rs27053 |
chr5:1470578(Fwd) |
intron_variant; NMD_transcript_variant; upstream_gene_variant |
rs27056 |
chr5:1473977(Fwd) |
intron_variant; NMD_transcript_variant |
rs31491 |
chr5:1477310(Fwd) |
downstream_gene_variant; intron_variant; NMD_transcript_variant |
rs2937652 |
chr5:1460132(Fwd) |
downstream_gene_variant; intron_variant; NMD_transcript_variant |