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: rs10500355
rs10500355
RBFOX1
3 0.925 0.040 16 7409346 intron variant T/A snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs10882165
rs10882165 		2 1.000 10 93164567 intergenic variant A/T snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs11145465
rs11145465
TJP2
2 1.000 9 69151677 missense variant C/A snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs11601239
rs11601239
GRIA4
2 1.000 11 105685872 intron variant C/G snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs12205363
rs12205363
LAMA2 ; LOC102723409
2 1.000 6 129513484 intron variant T/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs12229663
rs12229663
PTPRR
2 1.000 12 70856216 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1254319
rs1254319
C14orf39
3 1.000 14 60437039 missense variant G/A snv 0.35 0.36 0.700 1.000 1 2013 2013
dbSNP: rs12971120
rs12971120
CNDP2
2 1.000 18 74506788 intron variant A/G snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs14165
rs14165
CACNA1D ; CHDH
2 1.000 3 53813381 3 prime UTR variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1656404
rs1656404 		3 0.925 0.040 2 232515231 regulatory region variant G/A snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs17183295
rs17183295
MYO1D
4 1.000 17 32751254 intron variant C/T snv 0.14 0.700 1.000 1 2013 2013
dbSNP: rs17648524
rs17648524
RBFOX1
4 0.882 0.040 16 7409682 intron variant G/C snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs1881492
rs1881492
CHRNG
2 1.000 2 232542288 intron variant T/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs1960445
rs1960445 		2 1.000 4 81009660 intergenic variant C/T snv 0.81 0.700 1.000 1 2013 2013
dbSNP: rs2184971
rs2184971
PCCA
2 1.000 13 100165838 intron variant A/G snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs235770
rs235770 		2 1.000 20 6781118 downstream gene variant T/C snv 0.71 0.700 1.000 1 2013 2013
dbSNP: rs2969180
rs2969180
SHISA6
2 1.000 17 11504584 intron variant G/A snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs3138144
rs3138144
RDH5 ; BLOC1S1-RDH5
2 1.000 12 55720985 intron variant G/C snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs4778879
rs4778879
RASGRF1
2 1.000 15 79080533 intron variant A/G snv 0.42 0.700 1.000 1 2013 2013
dbSNP: rs4793501
rs4793501 		2 1.000 17 70722593 intergenic variant C/T snv 0.64 0.700 1.000 1 2013 2013
dbSNP: rs524952
rs524952 		6 0.827 0.040 15 34713685 intergenic variant T/A snv 0.50 0.700 1.000 1 2013 2013
dbSNP: rs634990
rs634990 		6 0.827 0.040 15 34713872 intergenic variant T/C snv 0.48 0.700 1.000 1 2010 2010
dbSNP: rs7042950
rs7042950
RORB
2 1.000 9 74534921 intron variant A/G snv 0.27 0.700 1.000 1 2013 2013
dbSNP: rs7084402
rs7084402 		4 0.925 0.040 10 58505644 intergenic variant A/G snv 0.51 0.700 1.000 1 2013 2013
dbSNP: rs7744813
rs7744813
KCNQ5
3 0.925 0.040 6 72933566 intron variant C/A snv 0.66 0.700 1.000 1 2013 2013