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: rs193922680
rs193922680
9 0.790 0.080 15 34793398 missense variant C/T snv 4.0E-06 7.0E-06 0.700 1.000 8 2000 2014
dbSNP: rs730880404
rs730880404
1 1.000 0.040 15 34791136 missense variant G/A snv 0.700 1.000 3 2012 2014
dbSNP: rs727504323
rs727504323
1 1.000 0.040 15 34792105 missense variant G/C snv 0.700 1.000 1 2017 2017
dbSNP: rs727504399
rs727504399
1 1.000 0.040 15 34794733 missense variant C/T snv 0.010 1.000 1 2019 2019