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: rs121434587
rs121434587
1 1.000 0.080 6 160069961 missense variant G/T snv 0.700 0
dbSNP: rs121434588
rs121434588
1 1.000 0.080 6 160070006 missense variant G/A snv 0.700 0
dbSNP: rs629849
rs629849
9 0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 0.010 < 0.001 1 2019 2019
dbSNP: rs642588
rs642588
2 0.925 0.120 6 159990235 intron variant A/G snv 0.83 0.010 < 0.001 1 2019 2019