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: rs10503899
rs10503899
1 1.000 0.040 8 32089718 intron variant A/G snv 0.33 0.700 1.000 1 2012 2012