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: rs62387962
rs62387962 		1 5 157871822 regulatory region variant G/T snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs6905986
rs6905986 		1 6 25627430 regulatory region variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs7771547
rs7771547 		1 6 36570618 regulatory region variant T/G snv 0.41 0.700 1.000 1 2016 2016
dbSNP: rs9473147
rs9473147 		2 6 47641856 regulatory region variant A/G snv 0.27 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: rs11684299
rs11684299 		1 2 226432279 intergenic variant C/G;T snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs11731274
rs11731274 		2 4 6889728 intergenic variant T/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs140426714
rs140426714 		1 8 19998334 intergenic variant ATTTTT/- delins 0.700 1.000 1 2016 2016
dbSNP: rs200092657
rs200092657
LOC101927086
1 9 70458030 intergenic variant G/- del 0.35 0.700 1.000 1 2016 2016
dbSNP: rs2364708
rs2364708 		1 10 22887797 intergenic variant G/A snv 0.39 0.700 1.000 1 2016 2016
dbSNP: rs2494979
rs2494979 		1 6 70637263 intergenic variant C/A;G snv 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: rs2857204
rs2857204 		1 6 32776570 intergenic variant G/T snv 0.35 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: rs4812056
rs4812056 		1 20 59098895 intergenic variant A/C snv 0.21 0.700 1.000 1 2016 2016
dbSNP: rs74847330
rs74847330
ARHGAP15
4 2 143074030 intergenic variant A/G snv 8.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs77124424
rs77124424 		1 20 59287932 intergenic variant T/C snv 2.5E-02 0.700 1.000 1 2016 2016
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