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rs869025615

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025615(-;-)
Make rs869025615(-;G)
Make rs869025615(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10142010
GeneVHL
is asnp
is mentioned by
dbSNPrs869025615
ebirs869025615
HLIrs869025615
Exacrs869025615
Varsomers869025615
Maprs869025615
PheGenIrs869025615
hapmaprs869025615
1000 genomesrs869025615
hgdprs869025615
ensemblrs869025615
gopubmedrs869025615
geneviewrs869025615
scholarrs869025615
googlers869025615
pharmgkbrs869025615
gwascentralrs869025615
openSNPrs869025615
23andMers869025615
23andMe allrs869025615
SNP Nexus

SNPshotrs869025615
SNPdbers869025615
MSV3drs869025615
GWAS Ctlgrs869025615
Max Magnitude0
ClinVar
Risk rs869025615(G;G)
Alt rs869025615(G;G)
Reference rs869025615(;)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183694dupG
CLNSRC
CLNACC RCV000208829.1,