rs869025640

Orientation

plus

Stabilized

plus

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

Make rs869025640(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

10146524

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs869025640
dbSNP (classic)	rs869025640
ClinGen	rs869025640
ebi	rs869025640
HLI	rs869025640
Exac	rs869025640
Gnomad	rs869025640
Varsome	rs869025640
LitVar	rs869025640
Map	rs869025640
PheGenI	rs869025640
Biobank	rs869025640
1000 genomes	rs869025640
hgdp	rs869025640
ensembl	rs869025640
geneview	rs869025640
scholar	rs869025640
google	rs869025640
pharmgkb	rs869025640
gwascentral	rs869025640
openSNP	rs869025640
23andMe	rs869025640
SNPshot	rs869025640
SNPdbe	rs869025640
MSV3d	rs869025640
GWAS Ctlg	rs869025640

Max Magnitude

7

ClinVar
Risk	rs869025640(-;-)
Alt	rs869025640(-;-)
Reference	Rs869025640(G;G)
Significance	Pathogenic
Disease	Von Hippel-Lindau syndrome
Variation	info
Gene	VHL
CLNDBN	Von Hippel-Lindau syndrome
Reversed	0
HGVS	NC_000003.11:g.10188208delG
CLNSRC
CLNACC	RCV000208786.1,