rs869025620

Orientation

plus

Stabilized

plus

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

Make rs869025620(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

10142068

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs869025620
dbSNP (classic)	rs869025620
ClinGen	rs869025620
ebi	rs869025620
HLI	rs869025620
Exac	rs869025620
Gnomad	rs869025620
Varsome	rs869025620
LitVar	rs869025620
Map	rs869025620
PheGenI	rs869025620
Biobank	rs869025620
1000 genomes	rs869025620
hgdp	rs869025620
ensembl	rs869025620
geneview	rs869025620
scholar	rs869025620
google	rs869025620
pharmgkb	rs869025620
gwascentral	rs869025620
openSNP	rs869025620
23andMe	rs869025620
SNPshot	rs869025620
SNPdbe	rs869025620
MSV3d	rs869025620
GWAS Ctlg	rs869025620

Max Magnitude

7

ClinVar
Risk	rs869025620(-;-)
Alt	rs869025620(-;-)
Reference	Rs869025620(T;T)
Significance	Pathogenic
Disease	Von Hippel-Lindau syndrome
Variation	info
Gene	VHL
CLNDBN	Von Hippel-Lindau syndrome
Reversed	0
HGVS	NC_000003.11:g.10183752delT
CLNSRC
CLNACC	RCV000208849.1,