rs869025623

Orientation

plus

Stabilized

plus

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

Make rs869025623(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

10142116

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs869025623
dbSNP (classic)	rs869025623
ClinGen	rs869025623
ebi	rs869025623
HLI	rs869025623
Exac	rs869025623
Gnomad	rs869025623
Varsome	rs869025623
LitVar	rs869025623
Map	rs869025623
PheGenI	rs869025623
Biobank	rs869025623
1000 genomes	rs869025623
hgdp	rs869025623
ensembl	rs869025623
geneview	rs869025623
scholar	rs869025623
google	rs869025623
pharmgkb	rs869025623
gwascentral	rs869025623
openSNP	rs869025623
23andMe	rs869025623
SNPshot	rs869025623
SNPdbe	rs869025623
MSV3d	rs869025623
GWAS Ctlg	rs869025623

Max Magnitude

7

ClinVar
Risk	rs869025623(-;-)
Alt	rs869025623(-;-)
Reference	Rs869025623(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.10183800delA
CLNSRC
CLNACC	RCV000208842.1,