rs869025642

Orientation

plus

Stabilized

plus

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

Make rs869025642(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

10146531

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs869025642
dbSNP (classic)	rs869025642
ClinGen	rs869025642
ebi	rs869025642
HLI	rs869025642
Exac	rs869025642
Gnomad	rs869025642
Varsome	rs869025642
LitVar	rs869025642
Map	rs869025642
PheGenI	rs869025642
Biobank	rs869025642
1000 genomes	rs869025642
hgdp	rs869025642
ensembl	rs869025642
geneview	rs869025642
scholar	rs869025642
google	rs869025642
pharmgkb	rs869025642
gwascentral	rs869025642
openSNP	rs869025642
23andMe	rs869025642
SNPshot	rs869025642
SNPdbe	rs869025642
MSV3d	rs869025642
GWAS Ctlg	rs869025642

Max Magnitude

7

ClinVar
Risk	rs869025642(G;G)
Alt	rs869025642(G;G)
Reference	Rs869025642(A;A)
Significance	Probable-Pathogenic
Disease	Von Hippel-Lindau syndrome
Variation	info
Gene	VHL
CLNDBN	Von Hippel-Lindau syndrome
Reversed	0
HGVS	NC_000003.11:g.10188215A>G
CLNSRC
CLNACC	RCV000208800.1,