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: rs6975977
rs6975977
MINDY4 ; INMT-MINDY4
1 1.000 0.080 7 30878216 intron variant G/A snv 7.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs7076156
rs7076156
ZNF365 ; LOC105378327
3 0.925 0.120 10 62655424 missense variant A/C;G snv 0.80 0.010 1.000 1 2014 2014
dbSNP: rs7206790
rs7206790
FTO
3 0.925 0.160 16 53763996 intron variant C/G snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs7277076
rs7277076
CLDN14 ; LOC105369301
2 1.000 0.080 21 36464675 intron variant T/C snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs7328064
rs7328064
DGKH
1 1.000 0.080 13 42171982 intron variant A/C snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs74956940
rs74956940
PKN1
1 1.000 0.080 19 14461154 intron variant C/G snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs756322971
rs756322971
CASR
9 0.763 0.240 3 122284955 missense variant C/A;G snv 0.010 1.000 1 2015 2015
dbSNP: rs9536314
rs9536314
KL
3 0.925 0.160 13 33054001 missense variant T/A;G snv 0.14 0.010 1.000 1 2019 2019