Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780830800
RIMS2
8 103885414 missense variant A/G snv 4.0E-06 1
rs1307973611
RIMS2
1.000 0.080 8 104014523 missense variant G/C;T snv 2
rs781230344
RIMS2
1.000 0.080 8 104014559 missense variant C/G snv 4.8E-05 2
rs1383969517
RIMS2
8 104014610 missense variant A/G snv 1
rs151091483
MYHAS ; MYH8
1.000 0.080 17 10409361 missense variant A/C;G;T snv 4.0E-06; 1.2E-05; 3.1E-04; 4.0E-06 1.3E-04 2
rs1475645821
RIMS2
8 104248715 missense variant G/A snv 4.0E-06 1
rs157077
GSTO2
1.000 0.080 10 104278136 intron variant T/C snv 0.45 0.53 3
rs138842024
DFFA
1 10469269 missense variant A/G snv 3.5E-03 3.1E-03 1
rs2498804
LOC102723342 ; SIVA1 ; LOC107987209
0.827 0.160 14 104766758 intron variant C/A;T snv 0.40 0.33 8
rs1057519804
AKT1
1.000 0.040 14 104776711 missense variant G/T snv 2
rs764931115
AKT1
0.925 0.200 14 104780148 missense variant T/C snv 4.0E-06 3
rs1380514442
AKT1
14 104780205 missense variant T/C snv 4.0E-06 1
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs12194974
LIN28B
6 104956323 intron variant G/A snv 9.0E-02 1
rs1535989 0.925 0.080 13 105370372 intergenic variant A/G;T snv 4
rs1467453450
FSD1L
0.882 0.080 9 105506513 missense variant A/G snv 7.0E-06 4
rs1968445
CDKN2D
19 10568564 synonymous variant C/G;T snv 0.95 1
rs2245214
ATG5
0.827 0.240 6 106214866 intron variant C/G snv 0.42 6
rs974296289
CKAP4
12 106247384 synonymous variant C/T snv 1
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs1273593548
PIK3CG
0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs750966175
QTRT1
19 10712181 missense variant C/T snv 4.0E-06 2.1E-05 1
rs4988483
SSTR5-AS1 ; SSTR5
0.752 0.240 16 1079010 missense variant C/A snv 3.7E-02 3.7E-02 11
rs1383147053
DLD
0.882 0.120 7 107901762 missense variant G/A snv 4
rs169068
SSTR5-AS1 ; SSTR5
0.742 0.280 16 1079872 missense variant C/T snv 0.54 0.50 12