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: rs13107325
rs13107325
SLC39A8
34 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.700 1.000 1 2019 2019
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: rs141424017
rs141424017 		3 1.000 0.080 7 115311376 intergenic variant -/CAA ins 0.700 1.000 1 2019 2019
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: rs1437396
rs1437396 		3 1.000 0.080 2 55278320 upstream gene variant C/G;T snv 0.700 1.000 1 2014 2014
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
dbSNP: rs1612735
rs1612735
ADH1B ; ADH1C
3 1.000 0.080 4 99336850 intron variant T/C snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs1614972
rs1614972
ADH1B ; ADH1C
4 0.925 0.160 4 99336998 intron variant C/T snv 0.38 0.700 1.000 1 2014 2014
dbSNP: rs1660895
rs1660895 		3 1.000 0.080 2 129236759 intergenic variant A/T snv 0.52 0.700 1.000 1 2014 2014
dbSNP: rs1693457
rs1693457
ADH1B
3 1.000 0.080 4 99315605 non coding transcript exon variant C/T snv 0.81 0.700 1.000 1 2014 2014
dbSNP: rs17028615
rs17028615
ADH4 ; LOC100507053
4 1.000 0.080 4 99150767 intron variant A/C;G snv 0.700 1.000 1 2014 2014
dbSNP: rs1709817
rs1709817
KCNJ6
3 1.000 0.080 21 37664047 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1709818
rs1709818
KCNJ6
3 1.000 0.080 21 37663909 intron variant T/C snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs1709819
rs1709819
KCNJ6
3 1.000 0.080 21 37663813 intron variant A/C snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs1709820
rs1709820
KCNJ6
3 1.000 0.080 21 37663669 intron variant A/C snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs1709826
rs1709826
KCNJ6
3 1.000 0.080 21 37677171 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1709832
rs1709832
KCNJ6
3 1.000 0.080 21 37665865 intron variant T/G snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs1709833
rs1709833
KCNJ6
3 1.000 0.080 21 37665503 intron variant A/G snv 0.57 0.700 1.000 1 2012 2012