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rs5030817

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Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs5030817(A;A)
Make rs5030817(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position10149786
GeneVHL
is asnp
is mentioned by
dbSNPrs5030817
ebirs5030817
HLIrs5030817
Exacrs5030817
Varsomers5030817
Maprs5030817
PheGenIrs5030817
hapmaprs5030817
1000 genomesrs5030817
hgdprs5030817
ensemblrs5030817
gopubmedrs5030817
geneviewrs5030817
scholarrs5030817
googlers5030817
pharmgkbrs5030817
gwascentralrs5030817
openSNPrs5030817
23andMers5030817
23andMe allrs5030817
SNP Nexus

SNPshotrs5030817
SNPdbers5030817
MSV3drs5030817
GWAS Ctlgrs5030817
Max Magnitude0


ClinVar
Risk rs5030817(A;A)
Alt rs5030817(A;A)
Reference rs5030817(G;G)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.10191470G>A; NC_000003.11:g.10191470G>C; NC_000003.11:g.10191470G>T
CLNSRC COSMIC
CLNACC RCV000036546.3, RCV000161080.1, RCV000208828.1, RCV000208870.1,