rs1064793878

Orientation

plus

Stabilized

plus

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

Chromosome

3

Position

10149874

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs1064793878
dbSNP (classic)	rs1064793878
ClinGen	rs1064793878
ebi	rs1064793878
HLI	rs1064793878
Exac	rs1064793878
Gnomad	rs1064793878
Varsome	rs1064793878
LitVar	rs1064793878
Map	rs1064793878
PheGenI	rs1064793878
Biobank	rs1064793878
1000 genomes	rs1064793878
hgdp	rs1064793878
ensembl	rs1064793878
geneview	rs1064793878
scholar	rs1064793878
google	rs1064793878
pharmgkb	rs1064793878
gwascentral	rs1064793878
openSNP	rs1064793878
23andMe	rs1064793878
SNPshot	rs1064793878
SNPdbe	rs1064793878
MSV3d	rs1064793878
GWAS Ctlg	rs1064793878

Max Magnitude

7

ClinVar
Risk	rs1064793878(C;C)
Alt	rs1064793878(C;C)
Reference	Rs1064793878(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	VHL
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.10191558T>C
CLNSRC
CLNACC	RCV000484822.1,