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: rs773243225
rs773243225
1 1.000 0.036 4 3532232 stop gained G/A snp 6.4E-06 0.700 4 2013 2016
dbSNP: rs10272030
rs10272030
HGF
1 1.000 0.036 7 81720907 intron variant G/A snp 0.85 0.010 1.000 1 2010 2010
dbSNP: rs10488
rs10488
1 1.000 0.036 11 102797291 synonymous variant C/G,T snp 4.0E-06; 5.7E-02 8.6E-02 0.010 1.000 1 2013 2013
dbSNP: rs10936538
rs10936538
1 1.000 0.036 3 167439281 intergenic variant C/A,T snp 0.41 0.010 1.000 1 2012 2012
dbSNP: rs12603825
rs12603825
1 1.000 0.036 17 1770111 intron variant G/A,T snp 0.30 0.010 1.000 1 2013 2013
dbSNP: rs131451
rs131451
1 1.000 0.036 22 23771357 intron variant C/T snp 0.82 0.010 1.000 1 2013 2013
dbSNP: rs1743
rs1743
HGF
1 1.000 0.036 7 81699165 3 prime UTR variant A/G,T snp 0.73 0.010 1.000 1 2010 2010
dbSNP: rs2239182
rs2239182
VDR
1 1.000 0.036 12 47861628 intron variant T/C snp 0.50 0.010 1.000 1 2011 2011
dbSNP: rs2853559
rs2853559
VDR
1 1.000 0.036 12 47889022 intron variant A/G snp 0.67 0.010 1.000 1 2011 2011
dbSNP: rs3819545
rs3819545
VDR
1 1.000 0.036 12 47871223 intron variant A/G snp 0.38 0.010 1.000 1 2011 2011
dbSNP: rs4732402
rs4732402
HGF
1 1.000 0.036 7 81701064 3 prime UTR variant C/A,G snp 0.72 0.010 1.000 1 2010 2010
dbSNP: rs498186
rs498186
1 1.000 0.036 11 102798914 intron variant A/C snp 0.40 0.010 1.000 1 2013 2013
dbSNP: rs644242
rs644242
1 1.000 0.036 11 31791253 non coding transcript exon variant C/A,G snp 5.7E-02 0.010 1.000 1 2011 2011
dbSNP: rs9642131
rs9642131
HGF
1 1.000 0.036 7 81740948 intron variant G/T snp 0.78 0.010 1.000 1 2010 2010
dbSNP: rs10453441
rs10453441
2 1.000 0.036 22 45967859 intron variant A/G snp 0.40 0.010 1.000 1 2016 2016
dbSNP: rs11225395
rs11225395
2 0.923 0.107 11 102725749 intron variant A/C,G snp 0.62 0.010 1.000 1 2013 2013
dbSNP: rs12536657
rs12536657
HGF
2 0.923 0.036 7 81720892 intron variant A/G snp 0.84 0.85 0.010 1.000 1 2010 2010
dbSNP: rs12716080
rs12716080
2 0.923 0.036 5 11166836 intron variant G/T snp 0.40 0.010 < 0.001 1 2011 2011
dbSNP: rs145100473
rs145100473
2 0.923 0.036 22 50524071 missense variant C/T snp 8.3E-04 1.3E-04 0.010 1.000 1 2013 2013
dbSNP: rs17122571
rs17122571
2 0.923 0.036 12 48027251 intergenic variant A/G snp 8.9E-02 0.010 1.000 1 2009 2009
dbSNP: rs2137277
rs2137277
2 1.000 0.036 8 40877143 intron variant A/G snp 0.21 0.010 1.000 1 2014 2014
dbSNP: rs2274755
rs2274755
2 1.000 0.036 20 46011053 splice region variant G/T snp 0.15 0.16 0.010 1.000 1 2013 2013
dbSNP: rs339501
rs339501
2 0.923 0.036 5 44365531 intron variant C/T snp 0.94 0.010 1.000 1 2013 2013
dbSNP: rs3741834
rs3741834
LUM
2 0.923 0.036 12 91111607 5 prime UTR variant G/A snp 3.2E-02 0.010 1.000 1 2009 2009
dbSNP: rs3759223
rs3759223
LUM
2 0.923 0.036 12 91113006 intergenic variant A/G snp 3.3E-02 0.010 1.000 1 2009 2009