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: rs11598177
rs11598177
1 1.000 0.040 10 101220399 regulatory region variant T/C snv 0.47 0.700 1.000 1 2011 2011
dbSNP: rs12432469
rs12432469
1 1.000 0.040 14 26807946 intron variant A/G snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs12432472
rs12432472
1 1.000 0.040 14 26807959 intron variant A/C snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs1322330
rs1322330
1 1.000 0.040 10 101231902 intron variant A/G snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs1322332
rs1322332
1 1.000 0.040 10 101222891 downstream gene variant T/C snv 0.50 0.700 1.000 1 2011 2011
dbSNP: rs1400180
rs1400180
1 1.000 0.040 3 129285 intron variant T/G snv 0.37 0.700 1.000 1 2011 2011
dbSNP: rs1400182
rs1400182
1 1.000 0.040 3 128928 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1407409
rs1407409
1 1.000 0.040 10 101225650 upstream gene variant T/C snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs1535462
rs1535462
1 1.000 0.040 10 101214115 TF binding site variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs1568097
rs1568097
1 1.000 0.040 3 138468 intron variant T/C snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs1588962
rs1588962
1 1.000 0.040 3 142352 intron variant T/C snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs17326792
rs17326792
1 1.000 0.040 3 131073 non coding transcript exon variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1878169
rs1878169
1 1.000 0.040 3 123429 intron variant A/T snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs200590764
rs200590764
1 1.000 0.040 10 101216904 intergenic variant -/T delins 6.6E-03 0.700 1.000 1 2011 2011
dbSNP: rs202193096
rs202193096
2 0.925 0.040 16 30089130 missense variant G/A snv 2.2E-04 1.0E-04 0.700 1.000 1 2015 2015
dbSNP: rs2281894
rs2281894
1 1.000 0.040 1 109267922 synonymous variant C/A snv 0.22 0.17 0.010 1.000 1 2017 2017
dbSNP: rs2393069
rs2393069
1 1.000 0.040 10 56359144 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs3950032
rs3950032
1 1.000 0.040 10 101214352 TF binding site variant A/C;G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs4684051
rs4684051
1 1.000 0.040 3 136842 intron variant A/G snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs594791
rs594791
1 1.000 0.040 10 101236039 intron variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs751819844
rs751819844
HGF
1 1.000 0.040 7 81705724 missense variant G/A snv 6.4E-05 2.8E-05 0.010 1.000 1 2019 2019
dbSNP: rs76319884
rs76319884
1 1.000 0.040 10 101216249 intergenic variant C/G snv 8.8E-02 0.700 1.000 1 2011 2011
dbSNP: rs7639674
rs7639674
1 1.000 0.040 3 130837 non coding transcript exon variant A/T snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs7914775
rs7914775
1 1.000 0.040 10 101216904 intergenic variant C/T snv 8.8E-02 0.700 1.000 1 2011 2011
dbSNP: rs965084
rs965084
1 1.000 0.040 3 125415 intron variant G/C snv 0.31 0.700 1.000 1 2011 2011