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: rs11642015
rs11642015
FTO
9 0.925 0.120 16 53768582 intron variant C/T snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs11725969
rs11725969
GUCY1A1
5 4 155705436 intron variant C/T snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs1173766
rs1173766 		5 5 32804422 intergenic variant T/C snv 0.57 0.700 1.000 1 2018 2018
dbSNP: rs12118370
rs12118370
ST7L
3 1 112605645 intron variant A/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs12129649
rs12129649
MOV10
4 1 112688881 5 prime UTR variant G/T snv 6.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs12209106
rs12209106 		2 6 1620807 downstream gene variant T/G snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs12416331
rs12416331
NT5C2
2 1.000 0.040 10 103169157 intron variant T/A snv 8.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs12421941
rs12421941
TLCD5
1 11 120323648 upstream gene variant A/G snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs12509595
rs12509595 		10 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs12579720
rs12579720
LINC02398
2 12 20020830 intron variant C/A;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12630213
rs12630213
FGD5
4 3 14912904 intron variant C/T snv 0.68 0.700 1.000 1 2018 2018
dbSNP: rs1265564
rs1265564
CUX2
4 1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs1275978
rs1275978
KCNK3
1 2 26700227 intron variant C/T snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs1275982
rs1275982
KCNK3
3 2 26696221 intron variant C/T snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs1275984
rs1275984 		4 2 26688641 upstream gene variant A/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs12790427
rs12790427
PCNX3
3 11 65617256 synonymous variant C/G;T snv 1.7E-05; 0.25 0.700 1.000 1 2018 2018
dbSNP: rs1290784
rs1290784
MECOM
6 3 169379112 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1290786
rs1290786
MECOM
1 3 169379593 intron variant C/T snv 0.42 0.700 1.000 1 2018 2018
dbSNP: rs12978472
rs12978472
INSR
5 19 7257979 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs13002573
rs13002573 		3 2 164058698 intron variant A/G snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs13125101
rs13125101 		6 4 80253438 TF binding site variant G/A snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs13209747
rs13209747 		5 6 126794309 intron variant C/G;T snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs13276026
rs13276026
PINX1 ; LOC102723313
3 8 10752445 intron variant G/A snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs13405173
rs13405173
PDE1A
3 2 182449087 intron variant A/C snv 8.8E-03 0.700 1.000 1 2018 2018
dbSNP: rs1379281
rs1379281
MYO9B
1 19 17078976 intron variant G/A snv 0.36 0.700 1.000 1 2018 2018