rs869025650

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;T)	7	Von Hippel-Lindau syndrome mutation

Make rs869025650(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

10146603

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs869025650
dbSNP (classic)	rs869025650
ClinGen	rs869025650
ebi	rs869025650
HLI	rs869025650
Exac	rs869025650
Gnomad	rs869025650
Varsome	rs869025650
LitVar	rs869025650
Map	rs869025650
PheGenI	rs869025650
Biobank	rs869025650
1000 genomes	rs869025650
hgdp	rs869025650
ensembl	rs869025650
geneview	rs869025650
scholar	rs869025650
google	rs869025650
pharmgkb	rs869025650
gwascentral	rs869025650
openSNP	rs869025650
23andMe	rs869025650
SNPshot	rs869025650
SNPdbe	rs869025650
MSV3d	rs869025650
GWAS Ctlg	rs869025650

Max Magnitude

7

ClinVar
Risk	rs869025650(A;A) rs869025650(T;T)
Alt	rs869025650(A;A) rs869025650(T;T)
Reference	Rs869025650(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.10188287G>T
CLNSRC
CLNACC	RCV000208850.1,