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: rs12460876
rs12460876
4 1.000 0.080 19 32865985 intron variant T/C snv 0.36 0.800 1.000 3 2010 2018
dbSNP: rs35975406
rs35975406
2 1.000 0.080 19 32866527 intron variant G/C;T snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs7252778
rs7252778
3 1.000 0.080 19 32869463 intron variant C/A;T snv 0.700 1.000 1 2018 2018