Source: GWASCAT ×
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: rs10498672
rs10498672
2 6 7797607 intron variant C/G snv 0.13 0.700 1.000 2 2019 2019
dbSNP: rs6923462
rs6923462
1 6 7800879 intron variant T/C snv 0.20 0.700 1.000 1 2014 2014