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rs121913346

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913346(A;A)
Make rs121913346(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position10149796
GeneVHL
is asnp
is mentioned by
dbSNPrs121913346
ebirs121913346
HLIrs121913346
Exacrs121913346
Varsomers121913346
Maprs121913346
PheGenIrs121913346
hapmaprs121913346
1000 genomesrs121913346
hgdprs121913346
ensemblrs121913346
gopubmedrs121913346
geneviewrs121913346
scholarrs121913346
googlers121913346
pharmgkbrs121913346
gwascentralrs121913346
openSNPrs121913346
23andMers121913346
23andMe allrs121913346
SNP Nexus

SNPshotrs121913346
SNPdbers121913346
MSV3drs121913346
GWAS Ctlgrs121913346
Max Magnitude0
ClinVar
Risk rs121913346(A,C;A,C)
Alt rs121913346(A,C;A,C)
Reference rs121913346(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Hereditary cancer-predisposing syndrome Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10191480T>C
CLNSRC
CLNACC RCV000161088.1, RCV000208846.1,