rs869025661

Orientation

plus

Stabilized

plus

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

Make rs869025661(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

10149794

Gene

VHL

is a	snp
is	mentioned by
dbSNP	rs869025661
dbSNP (classic)	rs869025661
ClinGen	rs869025661
ebi	rs869025661
HLI	rs869025661
Exac	rs869025661
Gnomad	rs869025661
Varsome	rs869025661
LitVar	rs869025661
Map	rs869025661
PheGenI	rs869025661
Biobank	rs869025661
1000 genomes	rs869025661
hgdp	rs869025661
ensembl	rs869025661
geneview	rs869025661
scholar	rs869025661
google	rs869025661
pharmgkb	rs869025661
gwascentral	rs869025661
openSNP	rs869025661
23andMe	rs869025661
SNPshot	rs869025661
SNPdbe	rs869025661
MSV3d	rs869025661
GWAS Ctlg	rs869025661

Max Magnitude

7

ClinVar
Risk	rs869025661(T;T)
Alt	rs869025661(T;T)
Reference	Rs869025661(-;-)
Significance	Probable-Pathogenic
Disease	Von Hippel-Lindau syndrome
Variation	info
Gene	VHL
CLNDBN	Von Hippel-Lindau syndrome
Reversed	0
HGVS	NC_000003.11:g.10191478dupT
CLNSRC
CLNACC	RCV000208814.1,