Source: GWASDB ×
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: rs12453334
rs12453334
1 1.000 0.080 17 39997220 intron variant C/T snv 0.28 0.700 1.000 1 2010 2010
dbSNP: rs8075668
rs8075668
1 1.000 0.080 17 39981370 intron variant C/T snv 0.51 0.700 1.000 1 2010 2010