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: rs10074523
rs10074523
2 1.000 0.080 5 132724891 intron variant C/A snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs17510339
rs17510339
1 1.000 0.080 5 132693722 3 prime UTR variant C/T snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs4705962
rs4705962
2 0.925 0.160 5 132693166 3 prime UTR variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs9327638
rs9327638
1 1.000 0.080 5 132734014 intron variant G/A;T snv 0.700 1.000 1 2019 2019