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: rs10740118
rs10740118
JMJD1C
1 10 63341447 intron variant G/C snv 0.38 0.700 1.000 1 2016 2016
dbSNP: rs10771511
rs10771511
FAR2 ; LOC100506606
1 12 29284284 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs10840293
rs10840293
SWAP70
2 1.000 0.040 11 9729649 intron variant G/A;C 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: rs11030122
rs11030122
STIM1
2 11 3865946 intron variant C/G snv 0.27 0.700 1.000 1 2016 2016
dbSNP: rs11062517
rs11062517
TSPAN9
1 12 3126673 intron variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11065961
rs11065961
ATXN2
1 12 111585263 intron variant G/A snv 0.57 0.700 1.000 1 2016 2016
dbSNP: rs11071720
rs11071720
TPM1 ; TPM1-AS
3 15 63049797 intron variant T/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs11082304
rs11082304
CABLES1
6 18 23141009 intron variant G/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11083766
rs11083766
MARK4 ; EXOC3L2 ; BLOC1S3
2 19 45212232 intron variant T/C snv 0.26 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: rs11124063
rs11124063
NCK2
1 2 105842350 intron variant T/C snv 0.68 0.700 1.000 1 2016 2016
dbSNP: rs111941366
rs111941366
RHCE
2 1 25409878 intron variant C/T snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs11576356
rs11576356
SKI
1 1 2302522 intron variant G/A snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs11620465
rs11620465
LRCH1
1 13 46676209 intron variant C/T snv 0.49 0.700 1.000 1 2016 2016
dbSNP: rs11646743
rs11646743
SEC14L5
1 16 4974040 intron variant G/A snv 0.42 0.700 1.000 1 2016 2016
dbSNP: rs11653357
rs11653357
AP2B1
2 17 35596588 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs116778355
rs116778355
DOCK10
1 2 224951925 intron variant A/T snv 1.5E-02 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: rs11765583
rs11765583
ELMO1
1 7 37401657 intron variant G/A snv 0.24 0.700 1.000 1 2016 2016
dbSNP: rs117672662
rs117672662
ACTN1
3 14 68958750 intron variant T/C snv 7.4E-03 0.700 1.000 1 2016 2016
dbSNP: rs117748422
rs117748422
GRTP1 ; GRTP1-AS1
1 13 113358194 intron variant C/T snv 3.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs12041331
rs12041331
PEAR1
11 0.776 0.200 1 156899922 intron variant G/A snv 0.19 0.700 1.000 1 2016 2016
dbSNP: rs12094497
rs12094497
FCER1G
1 1 161216513 intron variant G/A snv 8.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs12445050
rs12445050
PLCG2
3 16 81837364 intron variant C/T snv 9.6E-02 0.700 1.000 1 2016 2016