rs1064794037

Orientation

plus

Stabilized

plus

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

Chromosome

3

Position

10149805

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs1064794037
dbSNP (classic)	rs1064794037
ClinGen	rs1064794037
ebi	rs1064794037
HLI	rs1064794037
Exac	rs1064794037
Gnomad	rs1064794037
Varsome	rs1064794037
LitVar	rs1064794037
Map	rs1064794037
PheGenI	rs1064794037
Biobank	rs1064794037
1000 genomes	rs1064794037
hgdp	rs1064794037
ensembl	rs1064794037
geneview	rs1064794037
scholar	rs1064794037
google	rs1064794037
pharmgkb	rs1064794037
gwascentral	rs1064794037
openSNP	rs1064794037
23andMe	rs1064794037
SNPshot	rs1064794037
SNPdbe	rs1064794037
MSV3d	rs1064794037
GWAS Ctlg	rs1064794037

Max Magnitude

7

ClinVar
Risk	rs1064794037(-;-)
Alt	rs1064794037(-;-)
Reference	Rs1064794037(GCGAT;GCGAT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	VHL
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.10191489_10191493delGATGC
CLNSRC
CLNACC	RCV000480482.1,