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: rs6902119
rs6902119
1 0.882 0.160 6 167092303 intron variant T/C;G snv 0.700 1.000 2 2010 2012