Source: CURATED ×
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: rs142641502
rs142641502
CSTF3
3 0.925 0.040 11 33109861 intron variant T/C snv 8.0E-03 0.700 1.000 1 2016 2016
dbSNP: rs150175932
rs150175932
DCLK2
3 1.000 0.040 4 150101495 intron variant T/C snv 1.6E-02 0.700 1.000 1 2016 2016
dbSNP: rs17432675
rs17432675
LMOD1
2 1.000 0.040 1 201918593 intron variant T/C snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs189864513
rs189864513
LINC01618
3 0.925 0.040 4 52767390 intron variant T/C snv 1.9E-03 0.700 1.000 1 2016 2016
dbSNP: rs190783615
rs190783615 		3 0.925 0.040 X 142772620 intergenic variant T/C snv 9.3E-03 0.700 1.000 1 2016 2016
dbSNP: rs1908557
rs1908557 		3 0.925 0.040 4 89500202 intron variant T/C snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs34030812
rs34030812
ARHGAP15
2 1.000 0.040 2 143491336 intron variant T/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs35609938
rs35609938
LINC01122
2 1.000 0.040 2 58529594 intron variant T/C snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs384005
rs384005
MEF2C-AS2
2 5 88709286 intron variant T/C snv 0.70 0.700 1.000 1 2018 2018
dbSNP: rs4578918
rs4578918 		2 1.000 0.040 20 46093017 upstream gene variant T/C snv 0.77 0.700 1.000 1 2018 2018
dbSNP: rs7175083
rs7175083
LINGO1
2 1.000 0.040 15 77714500 intron variant T/C snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs73720034
rs73720034 		3 1.000 0.040 7 125794995 intergenic variant T/C snv 7.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs74338595
rs74338595
ERBB4
2 1.000 0.040 2 211885061 intron variant T/C snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs76923064
rs76923064 		2 1.000 0.040 2 156300636 downstream gene variant T/C snv 1.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs9858071
rs9858071
PLCL2
2 1.000 0.040 3 16803898 intron variant T/C snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs1490176
rs1490176
SORCS3
2 1.000 0.040 10 104800467 intron variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs17487484
rs17487484
DCC
2 1.000 0.040 18 53196913 intron variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs7939345
rs7939345 		3 1.000 0.040 11 47959016 intergenic variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs35909029
rs35909029
LINC02210-CRHR1
2 1.000 0.040 17 45774132 intron variant T/A;C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs13060816
rs13060816
BBX
2 1.000 0.040 3 107561639 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs1782179
rs1782179 		2 1.000 0.040 14 41224737 intergenic variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs188843168
rs188843168
ATP5MD
3 0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 0.700 1.000 1 2016 2016
dbSNP: rs2215939
rs2215939
LINC01122
2 1.000 0.040 2 58492312 intron variant T/A snv 0.57 0.700 1.000 1 2018 2018
dbSNP: rs73425402
rs73425402
NAV3
3 0.925 0.040 12 77503518 intron variant T/A snv 4.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs7583068
rs7583068
ERBB4
2 1.000 0.040 2 211769383 intron variant T/A snv 0.33 0.700 1.000 1 2018 2018