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: rs10272030
rs10272030
HGF
1 1.000 0.040 7 81720907 intron variant G/A snv 0.85 0.010 1.000 1 2010 2010
dbSNP: rs12536657
rs12536657
HGF
2 0.925 0.040 7 81720892 intron variant A/G snv 0.84 0.85 0.010 1.000 1 2010 2010
dbSNP: rs12716080
rs12716080
CTNND2
3 0.882 0.040 5 11166836 intron variant G/T snv 0.39 0.010 < 0.001 1 2011 2011
dbSNP: rs1743
rs1743
HGF
1 1.000 0.040 7 81699165 3 prime UTR variant A/G;T snv 0.010 1.000 1 2010 2010
dbSNP: rs4732402
rs4732402
HGF
1 1.000 0.040 7 81701064 3 prime UTR variant C/A;G snv 0.010 1.000 1 2010 2010
dbSNP: rs662702
rs662702
PAX6 ; ELP4
3 0.882 0.040 11 31787522 3 prime UTR variant C/T snv 0.15 0.010 1.000 1 2018 2018
dbSNP: rs6885224
rs6885224
CTNND2
3 0.882 0.040 5 11169833 intron variant C/A;T snv 0.010 < 0.001 1 2011 2011
dbSNP: rs9642131
rs9642131
HGF
1 1.000 0.040 7 81740948 intron variant G/T snv 0.78 0.010 1.000 1 2010 2010