Source: ALL
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: rs731236
rs731236
VDR
81 0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 0.010 1.000 1 2017 2017
dbSNP: rs7975232
rs7975232
VDR
56 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.010 1.000 1 2017 2017
dbSNP: rs9686714
rs9686714
WWC1
1 1.000 0.040 5 168426269 intron variant T/C snv 0.13 0.010 1.000 1 2017 2017
dbSNP: rs853974
rs853974 		3 0.882 0.120 6 126747838 intron variant T/C snv 0.77 0.020 1.000 2 2018 2018
dbSNP: rs1800872
rs1800872
IL10 ; IL19
119 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2018 2018
dbSNP: rs58542926
rs58542926
TM6SF2
42 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 0.010 1.000 1 2018 2018
dbSNP: rs738409
rs738409
PNPLA3
88 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.010 1.000 1 2018 2018
dbSNP: rs4620530
rs4620530
CHRM3 ; CHRM3-AS1
2 0.925 0.080 1 239900521 intron variant T/G snv 0.44 0.010 1.000 1 2020 2020