rs869025668

Orientation

plus

Stabilized

plus

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

Make rs869025668(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

10149964

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs869025668
dbSNP (classic)	rs869025668
ClinGen	rs869025668
ebi	rs869025668
HLI	rs869025668
Exac	rs869025668
Gnomad	rs869025668
Varsome	rs869025668
LitVar	rs869025668
Map	rs869025668
PheGenI	rs869025668
Biobank	rs869025668
1000 genomes	rs869025668
hgdp	rs869025668
ensembl	rs869025668
geneview	rs869025668
scholar	rs869025668
google	rs869025668
pharmgkb	rs869025668
gwascentral	rs869025668
openSNP	rs869025668
23andMe	rs869025668
SNPshot	rs869025668
SNPdbe	rs869025668
MSV3d	rs869025668
GWAS Ctlg	rs869025668

Max Magnitude

7

ClinVar
Risk	rs869025668(T;T)
Alt	rs869025668(T;T)
Reference	Rs869025668(G;G)
Significance	Probable-Pathogenic
Disease	Von Hippel-Lindau syndrome
Variation	info
Gene	VHL
CLNDBN	Von Hippel-Lindau syndrome
Reversed	0
HGVS	NC_000003.11:g.10191648G>T
CLNSRC
CLNACC	RCV000208844.1,