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: rs17651507
rs17651507
1 17 45981644 intron variant A/T snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs56087321
rs56087321
1 17 46007037 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs8070723
rs8070723
3 0.851 0.240 17 46003698 intron variant A/G snv 0.18 0.700 1.000 1 2019 2019