Source: GWASCAT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7916441
rs7916441
2 10 79165820 intron variant G/C snv 0.39 0.700 1.000 2 2010 2019
dbSNP: rs1658319
rs1658319
1 10 79165257 intron variant T/C snv 0.81 0.700 1.000 1 2019 2019
dbSNP: rs1815314
rs1815314
1 10 79169036 intron variant G/A;C;T snv 0.700 1.000 1 2014 2014
dbSNP: rs779933
rs779933
2 10 79158760 intron variant G/A snv 0.36 0.700 1.000 1 2015 2015
dbSNP: rs780151
rs780151
1 10 79171724 intron variant G/A snv 0.32 0.700 1.000 1 2013 2013