rs869025632

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(ACCGAGGTACG;ACCGAGGTACG)	0	common in clinvar
(TACCGAGGTACG;TACCGAGGTACG)	0	common in clinvar

Make rs869025632(-;-)

Make rs869025632(-;ACCGAGGTACG)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

10142182

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs869025632
dbSNP (classic)	rs869025632
ClinGen	rs869025632
ebi	rs869025632
HLI	rs869025632
Exac	rs869025632
Gnomad	rs869025632
Varsome	rs869025632
LitVar	rs869025632
Map	rs869025632
PheGenI	rs869025632
Biobank	rs869025632
1000 genomes	rs869025632
hgdp	rs869025632
ensembl	rs869025632
geneview	rs869025632
scholar	rs869025632
google	rs869025632
pharmgkb	rs869025632
gwascentral	rs869025632
openSNP	rs869025632
23andMe	rs869025632
SNPshot	rs869025632
SNPdbe	rs869025632
MSV3d	rs869025632
GWAS Ctlg	rs869025632

Max Magnitude

0

ClinVar
Risk	rs869025632(-;-)
Alt	rs869025632(-;-)
Reference	Rs869025632(ACCGAGGTACG;ACCGAGGTACG)
Significance	Pathogenic
Disease	Von Hippel-Lindau syndrome
Variation	info
Gene	VHL
CLNDBN	Von Hippel-Lindau syndrome
Reversed	0
HGVS	NC_000003.11:g.10183866_10183876delACCGAGGTACG
CLNSRC
CLNACC	RCV000208806.1,