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rs869025651

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025651(-;-)
Make rs869025651(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10146604
GeneVHL
is asnp
is mentioned by
dbSNPrs869025651
ebirs869025651
HLIrs869025651
Exacrs869025651
Varsomers869025651
Maprs869025651
PheGenIrs869025651
hapmaprs869025651
1000 genomesrs869025651
hgdprs869025651
ensemblrs869025651
gopubmedrs869025651
geneviewrs869025651
scholarrs869025651
googlers869025651
pharmgkbrs869025651
gwascentralrs869025651
openSNPrs869025651
23andMers869025651
23andMe allrs869025651
SNP Nexus

SNPshotrs869025651
SNPdbers869025651
MSV3drs869025651
GWAS Ctlgrs869025651
Max Magnitude0
ClinVar
Risk rs869025651(;)
Alt rs869025651(;)
Reference rs869025651(G;G)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10188288delG
CLNSRC
CLNACC RCV000208791.1,