Gene: VHL ×
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: rs398123481
rs398123481
VHL
2 1.000 0.120 3 10142103 missense variant C/G;T snv 0.700 1.000 19 1994 2016
dbSNP: rs397516441
rs397516441
VHL
4 0.882 0.200 3 10149790 missense variant A/G snv 0.700 1.000 13 1998 2014
dbSNP: rs5030622
rs5030622
VHL
3 0.925 0.160 3 10149809 stop gained C/A;G snv 0.700 1.000 13 1995 2016
dbSNP: rs869025618
rs869025618
VHL
2 1.000 0.120 3 10142061 missense variant T/C snv 0.700 1.000 11 2002 2015
dbSNP: rs5030822
rs5030822
VHL
3 0.925 0.160 3 10149856 missense variant T/A;C;G snv 0.700 1.000 10 1994 2008
dbSNP: rs5030818
rs5030818
VHL
4 0.882 0.280 3 10149804 stop gained C/G;T snv 0.700 1.000 9 1994 2016
dbSNP: rs5030830
rs5030830
VHL
3 0.925 0.160 3 10146526 missense variant T/C;G snv 0.700 1.000 9 1994 2012
dbSNP: rs730882035
rs730882035
VHL
7 0.807 0.200 3 10149805 missense variant G/A snv 0.700 1.000 9 1995 2016
dbSNP: rs104893825
rs104893825
VHL
2 1.000 0.120 3 10149819 missense variant G/T snv 0.700 1.000 8 1996 2010
dbSNP: rs104893826
rs104893826
VHL
4 0.882 0.200 3 10142038 missense variant G/A;C snv 0.700 1.000 7 1998 2014
dbSNP: rs193922613
rs193922613
VHL
3 0.925 0.160 3 10149847 missense variant A/G;T snv 0.700 1.000 7 2004 2014
dbSNP: rs730882034
rs730882034
VHL
3 0.925 0.160 3 10142104 missense variant C/G;T snv 0.700 1.000 6 1995 2016
dbSNP: rs786202787
rs786202787
VHL
2 1.000 0.120 3 10142085 missense variant A/C;G snv 0.700 1.000 6 1997 2014
dbSNP: rs104893830
rs104893830
VHL
3 0.925 0.160 3 10146561 missense variant G/C;T snv 0.700 1.000 5 1996 2014
dbSNP: rs1553620318
rs1553620318
VHL
1 3 10149810 missense variant C/T snv 0.700 1.000 5 2004 2016
dbSNP: rs193922609
rs193922609
VHL
2 1.000 0.120 3 10142167 missense variant G/A;C snv 0.700 1.000 5 1998 2012
dbSNP: rs864622109
rs864622109
VHL
2 1.000 0.120 3 10149878 stop gained C/G;T snv 0.700 1.000 5 1994 2013
dbSNP: rs1131690962
rs1131690962
VHL
1 3 10149829 missense variant T/C snv 0.700 1.000 4 2000 2015
dbSNP: rs5030825
rs5030825
VHL
1 3 10149906 stop gained C/T snv 0.700 1.000 4 1994 2013
dbSNP: rs869025615
rs869025615
VHL
2 1.000 0.120 3 10142009 frameshift variant G/-;GG delins 0.700 1.000 4 1995 2016
dbSNP: rs1131690954
rs1131690954
VHL
1 3 10146639 splice region variant A/G snv 0.700 1.000 3 2011 2015
dbSNP: rs1131690964
rs1131690964
VHL
2 1.000 0.120 3 10142124 frameshift variant G/- delins 0.700 1.000 3 1994 1998
dbSNP: rs121913346
rs121913346
VHL
3 0.925 0.240 3 10149796 missense variant T/A;C snv 0.700 1.000 3 1998 2009
dbSNP: rs587780077
rs587780077
VHL
2 1.000 0.120 3 10146618 missense variant G/A;C;T snv 0.700 1.000 3 1998 2014
dbSNP: rs869025655
rs869025655
VHL
3 0.925 0.160 3 10146625 missense variant T/C;G snv 0.700 1.000 3 1999 2007