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: rs3814231
rs3814231
1 1.000 0.040 10 113721259 intron variant C/T snv 0.23 0.800 1.000 1 2012 2012