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: rs1021469
rs1021469
AVIL
1 12 57814381 intron variant G/A snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs10215015
rs10215015
DGKB
1 7 14785984 intron variant A/G snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs10218999
rs10218999
LOC105376481
1 10 31076645 intron variant G/A snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs10232276
rs10232276
GRM8
1 7 126943467 intron variant T/C snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs10248878
rs10248878
OSBPL3
1 7 24869118 intron variant C/T snv 0.72 0.700 1.000 1 2018 2018
dbSNP: rs10268683
rs10268683
FBXL18
1 7 5511307 intron variant A/G snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs10268735
rs10268735
POU6F2 ; LOC105375239
1 7 39336423 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10276530
rs10276530
DGKB
1 7 14817300 intron variant T/C snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs1034811
rs1034811
ST6GAL2
1 2 106886868 intron variant C/T snv 0.72 0.700 1.000 1 2018 2018
dbSNP: rs10400054
rs10400054
SORCS3
1 10 105004435 intron variant A/C snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs10411759
rs10411759
KLF16
1 19 1857298 intron variant G/A snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs10432638
rs10432638
UBXN2A
1 2 23979642 intron variant C/A snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs10444280
rs10444280
LRRC4C
1 11 41134347 intron variant T/C snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs10455120
rs10455120
PHIP
1 6 79070050 intron variant T/G snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs10459501
rs10459501
MDGA2
1 14 47368546 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10459584
rs10459584
LINC01551 ; LINC02281
1 14 28803690 intron variant C/A snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs10490840
rs10490840
THRB-AS1 ; LOC107986011
1 3 24513213 intron variant G/A snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs10496090
rs10496090
PEX13
1 2 61026898 intron variant T/C snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs10496632
rs10496632
CNTNAP5
1 2 124256744 intron variant G/C snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs10497239
rs10497239
FIGN
1 2 163674795 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10499535
rs10499535
DNAH11
1 7 21650988 intron variant A/G snv 0.38 0.700 1.000 1 2018 2018
dbSNP: rs10510388
rs10510388
LMCD1-AS1
1 3 8215887 intron variant A/C snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs10512225
rs10512225
FAM120A
1 9 93464818 intron variant G/A snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs10512348
rs10512348
LINC01505
1 9 106684329 intron variant T/A snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs10734924
rs10734924
KNTC1
1 12 122534347 intron variant T/A;G snv 0.700 1.000 1 2018 2018