rs869025625

Orientation

plus

Stabilized

plus

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

Make rs869025625(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

10142143

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs869025625
dbSNP (classic)	rs869025625
ClinGen	rs869025625
ebi	rs869025625
HLI	rs869025625
Exac	rs869025625
Gnomad	rs869025625
Varsome	rs869025625
LitVar	rs869025625
Map	rs869025625
PheGenI	rs869025625
Biobank	rs869025625
1000 genomes	rs869025625
hgdp	rs869025625
ensembl	rs869025625
geneview	rs869025625
scholar	rs869025625
google	rs869025625
pharmgkb	rs869025625
gwascentral	rs869025625
openSNP	rs869025625
23andMe	rs869025625
SNPshot	rs869025625
SNPdbe	rs869025625
MSV3d	rs869025625
GWAS Ctlg	rs869025625

Max Magnitude

7

ClinVar
Risk	rs869025625(C;C)
Alt	rs869025625(C;C)
Reference	Rs869025625(-;-)
Significance	Pathogenic
Disease	Von Hippel-Lindau syndrome
Variation	info
Gene	VHL
CLNDBN	Von Hippel-Lindau syndrome
Reversed	0
HGVS	NC_000003.11:g.10183827dupC
CLNSRC
CLNACC	RCV000208817.1,