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: rs60286666
rs60286666
DOCK7
1 1 62655430 intron variant -/C ins 0.57 0.700 1.000 1 2016 2016
dbSNP: rs150647904
rs150647904
SSBP3
1 1 54373812 intron variant -/CAG delins 9.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs10638925
rs10638925
GP5
1 3 194399020 upstream gene variant -/GTAAAC delins 0.700 1.000 1 2016 2016
dbSNP: rs201738837
rs201738837
RWDD3 ; TLCD4-RWDD3 ; LOC101928118
1 1 95235667 intron variant -/T;TT delins 6.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs397712573
rs397712573
NRIP1
1 21 14999545 intron variant A/-;AA;AAA delins 0.700 1.000 1 2016 2016
dbSNP: rs10820606
rs10820606 		2 9 96430637 intergenic variant A/C snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs4812056
rs4812056 		1 20 59098895 intergenic variant A/C snv 0.21 0.700 1.000 1 2016 2016
dbSNP: rs79322592
rs79322592
TRIM58
1 1 247865478 intron variant A/C snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs13424581
rs13424581
DOCK10
1 2 224879779 intron variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs2723242
rs2723242
TLK1
1 2 171035869 intron variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs2165252
rs2165252
KALRN
1 3 124626515 intron variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10886430
rs10886430
GRK5
3 10 119250744 intron variant A/G snv 8.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs11121012
rs11121012
CAMTA1
2 1 7734229 intron variant A/G snv 0.62 0.700 1.000 1 2016 2016
dbSNP: rs11553699
rs11553699
RHOF ; TMEM120B
6 12 121779004 3 prime UTR variant A/G snv 9.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs11559982
rs11559982
COPZ1 ; RNU6-950P
2 12 54317790 non coding transcript exon variant A/G snv 0.68 0.700 1.000 1 2016 2016
dbSNP: rs1172149
rs1172149
TMCC2
2 1 205255630 intron variant A/G snv 0.51 0.700 1.000 1 2016 2016
dbSNP: rs141887296
rs141887296
LOC107985382
1 20 58951065 intron variant A/G snv 1.1E-03 0.700 1.000 1 2016 2016
dbSNP: rs1882
rs1882
MICA
1 6 31415134 3 prime UTR variant A/G snv 0.63 0.60 0.700 1.000 1 2016 2016
dbSNP: rs2278613
rs2278613
LOC145783 ; LOC105370833
1 15 56887102 non coding transcript exon variant A/G snv 0.41 0.700 1.000 1 2016 2016
dbSNP: rs2662368
rs2662368 		1 5 77685638 intergenic variant A/G snv 0.22 0.700 1.000 1 2016 2016
dbSNP: rs2780701
rs2780701
SYK
1 9 90804999 intron variant A/G snv 0.41 0.700 1.000 1 2016 2016
dbSNP: rs4290286
rs4290286
LOC105369623
1 12 6181375 intergenic variant A/G snv 0.33 0.700 1.000 1 2016 2016
dbSNP: rs571971615
rs571971615
CTSZ
1 20 59003687 intron variant A/G snv 1.5E-03 0.700 1.000 1 2016 2016
dbSNP: rs574551002
rs574551002
ZNF831
1 20 59210114 intron variant A/G snv 8.7E-04 0.700 1.000 1 2016 2016
dbSNP: rs59508494
rs59508494
TPM4
2 19 16100820 non coding transcript exon variant A/G snv 5.1E-02 0.700 1.000 1 2016 2016