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: rs10205350
rs10205350
GALNT14
1 1.000 0.040 2 30923631 intron variant G/T snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs10489525
rs10489525
CSDE1
1 1.000 0.040 1 114721064 intron variant G/A snv 0.32 0.800 1.000 1 2014 2014
dbSNP: rs11102800
rs11102800
TRIM33
2 1.000 0.040 1 114498310 intron variant C/T snv 0.58 0.800 1.000 1 2014 2014
dbSNP: rs11118968
rs11118968
RASSF5
1 1.000 0.040 1 206524916 intron variant G/A snv 7.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs11211996
rs11211996
GUCY1A2
1 1.000 0.040 11 106987949 intron variant T/C snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs11582563
rs11582563
TRIM33
1 1.000 0.040 1 114416918 intron variant G/A snv 0.14 0.800 1.000 1 2014 2014
dbSNP: rs11585926
rs11585926
TRIM33
3 1.000 0.040 1 114431068 intron variant T/C snv 0.22 0.800 1.000 1 2014 2014
dbSNP: rs11589568
rs11589568
TRIM33
1 1.000 0.040 1 114453702 intron variant T/C snv 0.14 0.800 1.000 1 2014 2014
dbSNP: rs12194182
rs12194182
SLC22A3
1 1.000 0.040 6 160413483 intron variant T/C snv 0.21 0.700 1.000 1 2012 2012
dbSNP: rs12331851
rs12331851
ZNF827
1 1.000 0.040 4 145928143 intron variant G/A snv 7.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs12726299
rs12726299
SLC22A15
1 1.000 0.040 1 115983051 intron variant G/A snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs13166776
rs13166776 		1 1.000 0.040 5 25971247 intron variant T/C snv 0.28 0.700 1.000 1 2009 2009
dbSNP: rs1429793
rs1429793
NELL1 ; LOC105376585
1 1.000 0.040 11 20904710 intron variant G/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1475531
rs1475531
MACROD2 ; MACROD2-AS1
1 1.000 0.040 20 14886776 intron variant G/T snv 0.62 0.700 1.000 1 2012 2012
dbSNP: rs16919315
rs16919315
TMEM132B
1 1.000 0.040 12 125599817 intron variant C/A;G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs17007739
rs17007739 		1 1.000 0.040 4 83920097 intron variant T/G snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs17134117
rs17134117
SDK1
1 1.000 0.040 7 3991432 intron variant C/T snv 9.1E-02 0.700 1.000 1 2013 2013
dbSNP: rs1718101
rs1718101
CNTNAP2
1 1.000 0.040 7 146425696 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs1879532
rs1879532
ERBB4
1 1.000 0.040 2 211574587 intron variant T/A;C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs1930165
rs1930165
PCDH15 ; LOC105378311
1 1.000 0.040 10 54542170 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs2056412
rs2056412
FAM135B
1 1.000 0.040 8 138401090 intron variant T/C snv 0.14 0.700 1.000 1 2013 2013
dbSNP: rs2150291
rs2150291
SYNE2
1 1.000 0.040 14 63864705 intron variant T/C snv 0.81 0.700 1.000 1 2012 2012
dbSNP: rs263025
rs263025
YEATS2 ; YEATS2-AS1
1 1.000 0.040 3 183809830 intron variant T/C snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs263035
rs263035
YEATS2
1 1.000 0.040 3 183805869 intron variant A/G snv 0.44 0.700 1.000 1 2012 2012
dbSNP: rs2836439
rs2836439
ERG
1 1.000 0.040 21 38493226 intron variant C/T snv 0.16 0.700 1.000 1 2012 2012