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: rs11735820
rs11735820
1 1.000 0.080 4 65633298 intron variant T/G snv 0.33 0.700 1.000 1 2011 2011
dbSNP: rs7659227
rs7659227
1 1.000 0.080 4 65630452 intron variant A/G snv 0.34 0.700 1.000 1 2011 2011