rs869025622

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;G)	7	Von Hippel-Lindau syndrome mutation
(G;G)	0	common in clinvar
(G;T)	7	Von Hippel-Lindau syndrome mutation

Make rs869025622(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

10142111

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs869025622
dbSNP (classic)	rs869025622
ClinGen	rs869025622
ebi	rs869025622
HLI	rs869025622
Exac	rs869025622
Gnomad	rs869025622
Varsome	rs869025622
LitVar	rs869025622
Map	rs869025622
PheGenI	rs869025622
Biobank	rs869025622
1000 genomes	rs869025622
hgdp	rs869025622
ensembl	rs869025622
geneview	rs869025622
scholar	rs869025622
google	rs869025622
pharmgkb	rs869025622
gwascentral	rs869025622
openSNP	rs869025622
23andMe	rs869025622
SNPshot	rs869025622
SNPdbe	rs869025622
MSV3d	rs869025622
GWAS Ctlg	rs869025622

Max Magnitude

7

ClinVar
Risk	rs869025622(T;T)
Alt	rs869025622(T;T)
Reference	Rs869025622(G;G)
Significance	Probable-Pathogenic
Disease	Von Hippel-Lindau syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	VHL
CLNDBN	Von Hippel-Lindau syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000003.11:g.10183795G>T
CLNSRC
CLNACC	RCV000208827.1, RCV000492552.1,