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: rs35795311
rs35795311
LINC02694
1 1.000 0.080 15 38706468 intron variant C/G snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs36094159
rs36094159
LINC02694
1 1.000 0.080 15 38706194 intron variant G/A snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs3773165
rs3773165
SLC6A6
1 1.000 0.080 3 14482762 intron variant G/A snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs3792686
rs3792686
NSG1
1 1.000 0.080 4 4391341 intron variant T/C snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs4384980
rs4384980 		1 1.000 0.080 3 182741281 upstream gene variant A/C snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs4610908
rs4610908 		1 1.000 0.080 X 35166418 intergenic variant G/A snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs6060124
rs6060124
GSS
1 1.000 0.080 20 34949094 intron variant C/A snv 0.27 0.700 1.000 1 2013 2013
dbSNP: rs6425323
rs6425323 		1 1.000 0.080 1 175155900 downstream gene variant C/T snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs6443238
rs6443238
SETD5
1 1.000 0.080 3 9407371 intron variant C/T snv 8.4E-02 0.700 1.000 1 2011 2011
dbSNP: rs6778524
rs6778524
PLCL2
1 1.000 0.080 3 16814451 intron variant T/C snv 8.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs7163869
rs7163869
LINC02694
1 1.000 0.080 15 38696190 intron variant G/C snv 0.26 0.700 1.000 1 2013 2013
dbSNP: rs7165988
rs7165988
LINC02694
1 1.000 0.080 15 38696614 non coding transcript exon variant C/G;T snv 0.26; 4.0E-06 0.700 1.000 1 2013 2013
dbSNP: rs7171233
rs7171233
LINC02694
1 1.000 0.080 15 38696559 intron variant T/A snv 0.26 0.26 0.700 1.000 1 2013 2013
dbSNP: rs7183893
rs7183893
LINC02694
1 1.000 0.080 15 38704780 intron variant A/C snv 0.23 0.700 1.000 1 2013 2013
dbSNP: rs7607774
rs7607774 		1 1.000 0.080 2 236520511 intergenic variant G/A snv 7.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs7777391
rs7777391 		1 1.000 0.080 7 117981823 intergenic variant A/G snv 0.60 0.700 1.000 1 2011 2011
dbSNP: rs9458121
rs9458121
MAP3K4
1 1.000 0.080 6 161101446 non coding transcript exon variant A/G snv 8.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs9847462
rs9847462 		1 1.000 0.080 3 164840807 intergenic variant A/G snv 0.14 0.700 1.000 1 2013 2013
dbSNP: rs994029
rs994029 		1 1.000 0.080 9 86760399 downstream gene variant C/T snv 0.71 0.700 1.000 1 2013 2013
dbSNP: rs1000579
rs1000579
STX18-AS1
3 1.000 0.080 4 4717767 intron variant A/G snv 0.44 0.800 1.000 2 2012 2017
dbSNP: rs1789891
rs1789891
ADH1B
3 1.000 0.080 4 99329262 intron variant C/A snv 0.13 0.820 1.000 2 2012 2019
dbSNP: rs2066702
rs2066702
ADH1B
3 0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 0.720 1.000 2 2014 2019
dbSNP: rs896543
rs896543
LOC107986001
3 1.000 0.080 2 236600564 intergenic variant G/A snv 0.33 0.800 1.000 2 2013 2014
dbSNP: rs10211296
rs10211296
CSRNP3
3 1.000 0.080 2 165633833 intron variant A/G snv 0.34 0.700 1.000 1 2017 2017
dbSNP: rs10483038
rs10483038
KCNJ6
3 1.000 0.080 21 37652469 intron variant T/C snv 0.26 0.700 1.000 1 2012 2012