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: rs13192566
rs13192566
1 1.000 0.080 6 169561539 intron variant G/C snv 9.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs71554396
rs71554396
1 1.000 0.080 6 169440978 intron variant TTTT/-;TTT;TTTTT delins 0.700 1.000 1 2017 2017