rs869025627

Orientation

plus

Stabilized

plus

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

Make rs869025627(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

10142156

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs869025627
dbSNP (classic)	rs869025627
ClinGen	rs869025627
ebi	rs869025627
HLI	rs869025627
Exac	rs869025627
Gnomad	rs869025627
Varsome	rs869025627
LitVar	rs869025627
Map	rs869025627
PheGenI	rs869025627
Biobank	rs869025627
1000 genomes	rs869025627
hgdp	rs869025627
ensembl	rs869025627
geneview	rs869025627
scholar	rs869025627
google	rs869025627
pharmgkb	rs869025627
gwascentral	rs869025627
openSNP	rs869025627
23andMe	rs869025627
SNPshot	rs869025627
SNPdbe	rs869025627
MSV3d	rs869025627
GWAS Ctlg	rs869025627

Max Magnitude

7

ClinVar
Risk	rs869025627(-;-)
Alt	rs869025627(-;-)
Reference	Rs869025627(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.10183840delT
CLNSRC
CLNACC	RCV000208801.1,