rs869025649

Orientation

plus

Stabilized

plus

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

Make rs869025649(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

10146592

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs869025649
dbSNP (classic)	rs869025649
ClinGen	rs869025649
ebi	rs869025649
HLI	rs869025649
Exac	rs869025649
Gnomad	rs869025649
Varsome	rs869025649
LitVar	rs869025649
Map	rs869025649
PheGenI	rs869025649
Biobank	rs869025649
1000 genomes	rs869025649
hgdp	rs869025649
ensembl	rs869025649
geneview	rs869025649
scholar	rs869025649
google	rs869025649
pharmgkb	rs869025649
gwascentral	rs869025649
openSNP	rs869025649
23andMe	rs869025649
SNPshot	rs869025649
SNPdbe	rs869025649
MSV3d	rs869025649
GWAS Ctlg	rs869025649

Max Magnitude

7

ClinVar
Risk	rs869025649(-;-)
Alt	rs869025649(-;-)
Reference	Rs869025649(TC;TC)
Significance	Pathogenic
Disease	Von Hippel-Lindau syndrome
Variation	info
Gene	VHL
CLNDBN	Von Hippel-Lindau syndrome
Reversed	0
HGVS	NC_000003.11:g.10188276_10188277delTC
CLNSRC
CLNACC	RCV000208805.1,