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rs869025657

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025657(C;C)
Make rs869025657(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10146637
GeneVHL
is asnp
is mentioned by
dbSNPrs869025657
ebirs869025657
HLIrs869025657
Exacrs869025657
Varsomers869025657
Maprs869025657
PheGenIrs869025657
hapmaprs869025657
1000 genomesrs869025657
hgdprs869025657
ensemblrs869025657
gopubmedrs869025657
geneviewrs869025657
scholarrs869025657
googlers869025657
pharmgkbrs869025657
gwascentralrs869025657
openSNPrs869025657
23andMers869025657
23andMe allrs869025657
SNP Nexus

SNPshotrs869025657
SNPdbers869025657
MSV3drs869025657
GWAS Ctlgrs869025657
Max Magnitude0
ClinVar
Risk rs869025657(C;C)
Alt rs869025657(C;C)
Reference rs869025657(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.10188321G>C
CLNSRC
CLNACC RCV000208796.1,