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: rs63750050
rs63750050
5 0.925 0.080 14 73198106 missense variant T/G snv 0.010 1.000 1 2010 2010
dbSNP: rs63750590
rs63750590
10 0.790 0.120 14 73186860 missense variant A/G snv 0.010 1.000 1 2010 2010
dbSNP: rs63750599
rs63750599
7 0.827 0.160 14 73170963 missense variant T/C snv 0.010 1.000 1 2019 2019
dbSNP: rs63750634
rs63750634
3 0.925 0.120 14 73192843 missense variant T/G snv 0.010 1.000 1 2003 2003
dbSNP: rs63751210
rs63751210
5 0.882 0.080 14 73186878 missense variant C/T snv 0.010 1.000 1 2001 2001