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: rs1057302
rs1057302
KIAA0040
1 1.000 0.080 1 175157287 3 prime UTR variant A/G snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs10913569
rs10913569
C1orf220
1 1.000 0.080 1 178548873 non coding transcript exon variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs11583322
rs11583322
STK40
1 1.000 0.080 1 36356711 intron variant T/C snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs11623335
rs11623335
TMEM260
1 1.000 0.080 14 56566358 intron variant G/A snv 0.85 0.700 1.000 1 2012 2012
dbSNP: rs11922615
rs11922615
SETD5
1 1.000 0.080 3 9416623 intron variant A/G snv 8.4E-02 0.700 1.000 1 2011 2011
dbSNP: rs12006002
rs12006002
ADAMTSL1
1 1.000 0.080 9 18166901 intron variant C/T snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs12392447
rs12392447
RN7SL697P
1 1.000 0.080 X 154496001 non coding transcript exon variant A/G snv 0.700 1.000 1 2009 2009
dbSNP: rs12427267
rs12427267
LOC105369901
1 1.000 0.080 12 91930196 intergenic variant A/G snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs12489456
rs12489456
SLC6A6
1 1.000 0.080 3 14459666 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs12901215
rs12901215
LINC02694
1 1.000 0.080 15 38700692 intron variant G/A snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs12903120
rs12903120
LINC02694
1 1.000 0.080 15 38695896 intron variant G/T snv 0.26 0.700 1.000 1 2013 2013
dbSNP: rs12916379
rs12916379
LINC02694
1 1.000 0.080 15 38699319 non coding transcript exon variant A/G snv 0.22 0.700 1.000 1 2013 2013
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: rs17616845
rs17616845 		1 1.000 0.080 7 12741918 intron variant T/C snv 0.15 0.700 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: 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: 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: rs34141940
rs34141940
LINC02694
1 1.000 0.080 15 38697456 intron variant G/A snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs34281605
rs34281605
LINC02694
1 1.000 0.080 15 38697473 intron variant G/A snv 0.26 0.700 1.000 1 2013 2013
dbSNP: rs34356257
rs34356257
LINC02694
1 1.000 0.080 15 38697404 intron variant T/A;C snv 0.26 0.700 1.000 1 2013 2013
dbSNP: rs35024396
rs35024396
LINC02694
1 1.000 0.080 15 38697569 intron variant G/A snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs35102843
rs35102843
LINC02694
1 1.000 0.080 15 38695906 intron variant C/A snv 0.26 0.700 1.000 1 2013 2013