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: rs1552224
rs1552224
1 1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 0.820 1.000 5 2010 2018
dbSNP: rs11602873
rs11602873
1 1.000 0.080 11 72749717 intron variant A/T snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs56200889
rs56200889
1 1.000 0.080 11 72697010 missense variant G/C snv 0.25 0.25 0.700 1.000 1 2018 2018
dbSNP: rs76550717
rs76550717
1 1.000 0.080 11 72717127 intron variant A/G snv 0.14 0.700 1.000 1 2019 2019