rs869025648

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs869025648(A;G)

Make rs869025648(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

10146587

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs869025648
dbSNP (classic)	rs869025648
ClinGen	rs869025648
ebi	rs869025648
HLI	rs869025648
Exac	rs869025648
Gnomad	rs869025648
Varsome	rs869025648
LitVar	rs869025648
Map	rs869025648
PheGenI	rs869025648
Biobank	rs869025648
1000 genomes	rs869025648
hgdp	rs869025648
ensembl	rs869025648
geneview	rs869025648
scholar	rs869025648
google	rs869025648
pharmgkb	rs869025648
gwascentral	rs869025648
openSNP	rs869025648
23andMe	rs869025648
SNPshot	rs869025648
SNPdbe	rs869025648
MSV3d	rs869025648
GWAS Ctlg	rs869025648

Max Magnitude

0

ClinVar
Risk	rs869025648(G;G)
Alt	rs869025648(G;G)
Reference	Rs869025648(A;A)
Significance	Probable-Pathogenic
Disease	Von Hippel-Lindau syndrome Hereditary cancer-predisposing syndrome Erythrocytosis
Variation	info
Gene	VHL
CLNDBN	Von Hippel-Lindau syndrome Hereditary cancer-predisposing syndrome Erythrocytosis, familial, 2
Reversed	0
HGVS	NC_000003.11:g.10188271A>G
CLNSRC
CLNACC	RCV000208865.1, RCV000216698.1, RCV000469600.1,