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rs869025655

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025655(G;G)
Make rs869025655(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10146625
GeneVHL
is asnp
is mentioned by
dbSNPrs869025655
ebirs869025655
HLIrs869025655
Exacrs869025655
Varsomers869025655
Maprs869025655
PheGenIrs869025655
hapmaprs869025655
1000 genomesrs869025655
hgdprs869025655
ensemblrs869025655
gopubmedrs869025655
geneviewrs869025655
scholarrs869025655
googlers869025655
pharmgkbrs869025655
gwascentralrs869025655
openSNPrs869025655
23andMers869025655
23andMe allrs869025655
SNP Nexus

SNPshotrs869025655
SNPdbers869025655
MSV3drs869025655
GWAS Ctlgrs869025655
Max Magnitude0
ClinVar
Risk rs869025655(G;G)
Alt rs869025655(G;G)
Reference rs869025655(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.10188309T>G
CLNSRC
CLNACC RCV000208823.1,