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: rs1332184
rs1332184
MIR31HG
1 1.000 0.080 9 21504204 intron variant A/C;G;T snv 0.010 1.000 1 2007 2007
dbSNP: rs142427338
rs142427338
ALDH1B1
1 1.000 0.080 9 38396880 stop gained C/T snv 1.0E-03; 4.0E-06 1.0E-03 0.010 1.000 1 2017 2017
dbSNP: rs1427074798
rs1427074798
PKD2L1
1 1.000 0.080 10 100297067 synonymous variant A/G snv 4.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs1439047
rs1439047
NTRK2
1 1.000 0.080 9 84713003 intron variant A/G snv 0.50 0.010 1.000 1 2017 2017
dbSNP: rs1443547
rs1443547
SLC6A5
1 1.000 0.080 11 20601429 missense variant G/A snv 0.37 0.38 0.010 1.000 1 2009 2009
dbSNP: rs1451724
rs1451724
RHOG
1 1.000 0.080 11 3835438 intron variant G/A snv 0.39 0.700 1.000 1 2013 2013
dbSNP: rs17028719
rs17028719 		1 1.000 0.080 1 5734948 intergenic variant A/G snv 4.8E-02 0.700 1.000 1 2011 2011
dbSNP: rs172677
rs172677
GRIN2B
1 1.000 0.080 12 13944536 intron variant A/G snv 0.63 0.010 1.000 1 2017 2017
dbSNP: rs17616845
rs17616845 		1 1.000 0.080 7 12741918 intron variant T/C snv 0.15 0.700 1.000 1 2013 2013
dbSNP: rs17689966
rs17689966
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
1 1.000 0.080 17 45833089 intron variant G/A snv 0.63 0.56 0.010 1.000 1 2013 2013
dbSNP: rs17754467
rs17754467
NRXN3
1 1.000 0.080 14 78156180 intergenic variant A/G snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs17862325
rs17862325
GRM8 ; GRM8-AS1
1 1.000 0.080 7 127214599 intron variant A/G snv 0.21 0.010 1.000 1 2015 2015
dbSNP: rs1800564
rs1800564
LEP
1 1.000 0.080 7 128254587 missense variant G/A;T snv 1.5E-04; 4.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs1869324
rs1869324
THSD7B
1 1.000 0.080 2 137469872 intron variant G/A snv 7.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs188227250
rs188227250
LINC00861
1 1.000 0.080 8 126201154 intron variant G/A snv 5.4E-02 0.010 1.000 1 2019 2019
dbSNP: rs1890881
rs1890881
RABGAP1L
1 1.000 0.080 1 174207785 intron variant T/C snv 0.12 0.010 1.000 1 2019 2019
dbSNP: rs1912461
rs1912461 		1 1.000 0.080 15 36052338 intron variant T/C snv 3.3E-02 0.010 1.000 1 2019 2019
dbSNP: rs1943418
rs1943418 		1 1.000 0.080 18 59812296 intergenic variant T/C snv 0.76 0.010 1.000 1 2007 2007
dbSNP: rs1986644
rs1986644
OBI1-AS1
1 1.000 0.080 13 78409942 intron variant G/A;C snv 0.010 1.000 1 2011 2011
dbSNP: rs1995364
rs1995364 		1 1.000 0.080 5 10903669 intergenic variant A/G snv 0.62 0.700 1.000 1 2013 2013
dbSNP: rs2132157
rs2132157
LINC02694
1 1.000 0.080 15 38700346 intron variant A/G snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs2172835
rs2172835
LINC02694
1 1.000 0.080 15 38697970 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2239670
rs2239670
CARTPT
1 1.000 0.080 5 71719676 non coding transcript exon variant A/G;T snv 0.010 1.000 1 2004 2004
dbSNP: rs2269655
rs2269655
KIAA0040
1 1.000 0.080 1 175166468 intron variant C/A;T snv 0.010 1.000 1 2011 2011
dbSNP: rs2276305
rs2276305
HTR3B
1 1.000 0.080 11 113932382 synonymous variant G/A;C;T snv 7.7E-02; 2.8E-03; 5.2E-05 0.010 1.000 1 2013 2013