rs_ID |
Location |
Functional Annotation |
rs11218091 |
chr11:120848006(Fwd) |
intron_variant |
rs524792 |
chr11:120830413(Fwd) |
intron_variant; nc_transcript_variant |
rs10750178 |
chr11:120823528(Fwd) |
intron_variant; nc_transcript_variant |
rs11217941 |
chr11:120531656(Fwd) |
intron_variant; nc_transcript_variant |
rs582718 |
chr11:120823104(Fwd) |
intron_variant; nc_transcript_variant |
rs6589829 |
chr11:120530973(Fwd) |
intron_variant; nc_transcript_variant; splice_region_variant |
rs684913 |
chr11:120819562(Fwd) |
intron_variant; nc_transcript_variant |
rs471403 |
chr11:120816277(Fwd) |
intron_variant; nc_transcript_variant |
rs609989 |
chr11:120814342(Fwd) |
intron_variant; nc_transcript_variant |
rs511939 |
chr11:120813715(Fwd) |
intron_variant; nc_transcript_variant |
rs580711 |
chr11:120809198(Fwd) |
intron_variant; nc_transcript_variant; upstream_gene_variant |
rs509566 |
chr11:120801460(Fwd) |
intron_variant; nc_transcript_variant |
rs2850807 |
chr11:120797893(Fwd) |
intron_variant; nc_transcript_variant |
rs2852241 |
chr11:120797584(Fwd) |
intron_variant; nc_transcript_variant |
rs10892591 |
chr11:120521766(Fwd) |
intron_variant; nc_transcript_variant |
rs1893907 |
chr11:120524884(Fwd) |
intron_variant; nc_transcript_variant |
rs4935749 |
chr11:120518929(Fwd) |
intron_variant; nc_transcript_variant |
rs4936536 |
chr11:120521485(Fwd) |
intron_variant; nc_transcript_variant |
rs6589826 |
chr11:120517643(Fwd) |
intron_variant; nc_transcript_variant |
rs6589827 |
chr11:120517844(Fwd) |
intron_variant; nc_transcript_variant |
rs1317514 |
chr11:120513914(Fwd) |
intron_variant; nc_transcript_variant |
rs2000874 |
chr11:120516717(Fwd) |
intron_variant; nc_transcript_variant |
rs7939968 |
chr11:120531435(Fwd) |
intron_variant; nc_transcript_variant |
rs1893906 |
chr11:120525032(Fwd) |
intron_variant; nc_transcript_variant |
rs4936538 |
chr11:120530316(Fwd) |
intron_variant; nc_transcript_variant |