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: rs1000579
rs1000579
STX18-AS1
3 1.000 0.080 4 4717767 intron variant A/G snv 0.44 0.700 1.000 2 2012 2017
dbSNP: rs1789891
rs1789891
ADH1B
4 1.000 0.080 4 99329262 intron variant C/A snv 0.13 0.700 1.000 2 2012 2017
dbSNP: rs10196867
rs10196867
CTNNA2
5 0.925 0.080 2 79751234 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10211296
rs10211296
CSRNP3
3 1.000 0.080 2 165633833 intron variant A/G snv 0.34 0.700 1.000 1 2017 2017
dbSNP: rs10483038
rs10483038
KCNJ6
3 1.000 0.080 21 37652469 intron variant T/C snv 0.26 0.700 1.000 1 2012 2012
dbSNP: rs11066001
rs11066001
BRAP
15 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.700 1.000 1 2019 2019
dbSNP: rs11075992
rs11075992
FTO
3 1.000 0.080 16 53786154 intron variant T/C snv 0.41 0.700 1.000 1 2019 2019
dbSNP: rs111372083
rs111372083
KCNJ6
3 1.000 0.080 21 37638374 intron variant C/A;T snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs1154433
rs1154433
ADH1B
3 1.000 0.080 4 99332551 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs115460205
rs115460205
FSTL5
3 1.000 0.080 4 161890417 intron variant C/T snv 4.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs11681792
rs11681792
NRXN1
4 1.000 0.080 2 49957256 intron variant C/T snv 0.12 0.700 1.000 1 2013 2013
dbSNP: rs11825659
rs11825659
IGSF9B
4 0.925 0.080 11 133925624 intron variant A/G snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs12482570
rs12482570
KCNJ6 ; LOC107985507
3 1.000 0.080 21 37705475 intron variant A/G snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs12544026
rs12544026
NCALD
4 0.925 0.080 8 101819970 intron variant G/A snv 0.85 0.700 1.000 1 2017 2017
dbSNP: rs12639833
rs12639833
ADH1B ; ADH1C
3 1.000 0.080 4 99346215 intron variant C/T snv 0.31 0.700 1.000 1 2014 2014
dbSNP: rs1316543
rs1316543
GRK5
3 1.000 0.080 10 119445148 intron variant G/A snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs139438618
rs139438618
SEMA3A
5 0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs1399590
rs1399590
KCNJ6
3 1.000 0.080 21 37681768 intron variant G/A snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs1399591
rs1399591
KCNJ6
3 1.000 0.080 21 37681654 intron variant C/T snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs1399592
rs1399592
KCNJ6
3 1.000 0.080 21 37681559 intron variant T/A;G snv 0.52 0.700 1.000 1 2012 2012
dbSNP: rs1421085
rs1421085
FTO
28 0.752 0.280 16 53767042 intron variant T/C snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs147247472
rs147247472
AGBL4 ; AGBL4-IT1
5 0.925 0.080 1 49441901 intron variant G/A snv 7.3E-04 0.700 1.000 1 2019 2019
dbSNP: rs1475839
rs1475839
KCNJ6
3 1.000 0.080 21 37649639 intron variant C/T snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs1515050
rs1515050
KCNJ6
3 1.000 0.080 21 37630840 intron variant T/C snv 0.75 0.700 1.000 1 2012 2012
dbSNP: rs1515056
rs1515056
KCNJ6 ; LOC107985507
3 1.000 0.080 21 37710283 intron variant C/G;T snv 0.28 0.700 1.000 1 2012 2012