rs869025646

Orientation

plus

Stabilized

plus

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

Make rs869025646(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

10146575

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs869025646
dbSNP (classic)	rs869025646
ClinGen	rs869025646
ebi	rs869025646
HLI	rs869025646
Exac	rs869025646
Gnomad	rs869025646
Varsome	rs869025646
LitVar	rs869025646
Map	rs869025646
PheGenI	rs869025646
Biobank	rs869025646
1000 genomes	rs869025646
hgdp	rs869025646
ensembl	rs869025646
geneview	rs869025646
scholar	rs869025646
google	rs869025646
pharmgkb	rs869025646
gwascentral	rs869025646
openSNP	rs869025646
23andMe	rs869025646
SNPshot	rs869025646
SNPdbe	rs869025646
MSV3d	rs869025646
GWAS Ctlg	rs869025646

Max Magnitude

7

ClinVar
Risk	rs869025646(-;-)
Alt	rs869025646(-;-)
Reference	Rs869025646(A;A)
Significance	Pathogenic
Disease	Von Hippel-Lindau syndrome
Variation	info
Gene	VHL
CLNDBN	Von Hippel-Lindau syndrome
Reversed	0
HGVS	NC_000003.11:g.10188259delA
CLNSRC
CLNACC	RCV000208816.1,