Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10008637
SHROOM3
4 76492991 intron variant T/A;C snv 0.35 2
rs10032549
SHROOM3
4 76476862 intron variant A/G snv 0.43 1
rs10066990 5 34509720 regulatory region variant G/A snv 0.30 1
rs10084572
LOC105372829
1.000 0.040 21 43992991 downstream gene variant T/A;C;G snv 3
rs10086569
SLC7A13
8 86234980 intron variant C/T snv 0.26 1
rs10096421
XKR6
8 10974358 intron variant T/G snv 0.60 1
rs10098664
BLK
8 11559984 non coding transcript exon variant T/A;C snv 1
rs10102889
NRG1
8 32578102 intron variant C/G snv 9.0E-02 1
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 5
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs10120859
TMEM252-DT ; TMEM252
9 68541379 intron variant T/C snv 0.17 1
rs10122824
QSOX2
9 136218015 intron variant T/C;G snv 0.68 1
rs10127790
SORT1
1 109348511 intron variant C/T snv 0.63 2
rs10142839
DIO2-AS1
14 80411775 intron variant G/A snv 0.33 1
rs10158537
SDCCAG8
1 243324884 intron variant C/G;T snv 1
rs10159261
DNAJC16 ; AGMAT
1 15586492 non coding transcript exon variant G/T snv 0.30 1
rs10179584
LOC105373454
2 18497405 intron variant T/C snv 0.42 1
rs10181201
SPTBN1
2 54572037 intron variant A/G;T snv 1
rs10186482
NEB
2 151625463 intron variant A/G snv 0.51 1
rs10189682
LOC101928278
2 216781832 intron variant G/A;T snv 1
rs10197255
LOC105374786
2 67647421 intron variant T/A;C snv 1
rs10206899
ALMS1P1
2 73673773 intron variant T/C;G snv 0.21; 3.9E-05 3
rs10223666
LOC105375069 ; LOC107986598
1.000 0.040 6 43837765 intron variant G/A;C snv 3
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 9