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: rs10030601
rs10030601
IQCM
1 1.000 0.040 4 149804060 intron variant T/C snv 0.22 0.800 1.000 1 2012 2012
dbSNP: rs11214136
rs11214136
BCO2
1 1.000 0.040 11 112211286 intron variant T/C snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs1178326
rs1178326
HDAC9
2 1.000 0.040 7 18195234 intron variant T/C snv 3.9E-02 0.700 1.000 1 2015 2015
dbSNP: rs12059546
rs12059546
CHRM3
1 0.925 0.040 1 239806797 intron variant A/G snv 0.30 0.800 1.000 1 2012 2012
dbSNP: rs12668095
rs12668095
LOC105375268
2 1.000 0.040 7 47036178 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs13287547
rs13287547
C9orf92
2 1.000 0.040 9 16286892 intron variant A/G snv 0.32 0.700 1.000 1 2015 2015
dbSNP: rs1394074
rs1394074
OLFML3
1 1.000 0.040 1 114005041 intron variant C/G snv 2.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs141860749
rs141860749
SYT2
2 1.000 0.040 1 202668176 intron variant C/A snv 2.7E-04 0.700 1.000 1 2015 2015
dbSNP: rs1429264
rs1429264
COTL1
2 1.000 0.040 16 84589878 intron variant T/C snv 0.28 0.700 1.000 1 2015 2015
dbSNP: rs148173957
rs148173957
LOC105378976
2 1.000 0.040 5 56078195 intron variant TT/- del 8.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs39861
rs39861
MAST4
1 1.000 0.040 5 66856430 intron variant A/G snv 0.25 0.800 1.000 1 2012 2012
dbSNP: rs55949311
rs55949311
LOC105370210
2 1.000 0.040 13 53557781 intron variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs62270313
rs62270313
EPHB1
2 1.000 0.040 3 134930924 intron variant T/C snv 0.16 0.700 1.000 1 2015 2015
dbSNP: rs631844
rs631844
LINC02109 ; LOC107986410
2 1.000 0.040 5 29054513 intron variant C/T snv 0.48 0.700 1.000 1 2015 2015
dbSNP: rs6432877
rs6432877
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166142257 intron variant C/A;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6732655
rs6732655
SCN1A ; SCN1A-AS1
1 1.000 0.040 2 166038556 intron variant A/T snv 0.74 0.700 1.000 1 2014 2014
dbSNP: rs72700966
rs72700966
PTPRD
1 1.000 0.040 9 10505224 intron variant C/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs7328626
rs7328626 		2 1.000 0.040 13 53576772 intron variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs79007183
rs79007183
CRAMP1
2 1.000 0.040 16 1655793 intron variant G/A snv 2.8E-05 0.700 1.000 1 2015 2015
dbSNP: rs9596837
rs9596837 		2 1.000 0.040 13 53683928 intron variant T/C snv 0.11 0.700 1.000 1 2015 2015
dbSNP: rs9596863
rs9596863
LINC00558
2 1.000 0.040 13 53860512 intron variant T/G snv 0.11 0.700 1.000 1 2015 2015
dbSNP: rs10496964
rs10496964 		1 0.925 0.040 2 144602342 intergenic variant C/T snv 0.12 0.800 1.000 1 2012 2012
dbSNP: rs111577701
rs111577701 		1 1.000 0.040 3 168143620 intergenic variant C/T snv 0.13 0.700 1.000 1 2014 2014
dbSNP: rs11663316
rs11663316 		2 1.000 0.040 18 9027916 intergenic variant T/A snv 0.34 0.700 1.000 1 2015 2015
dbSNP: rs118166657
rs118166657 		2 1.000 0.040 14 63580544 intergenic variant C/G snv 1.3E-02 0.700 1.000 1 2015 2015