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rs5030835

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs5030835(C;G)
Make rs5030835(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position10149848
GeneVHL
is asnp
is mentioned by
dbSNPrs5030835
ebirs5030835
HLIrs5030835
Exacrs5030835
Varsomers5030835
Maprs5030835
PheGenIrs5030835
hapmaprs5030835
1000 genomesrs5030835
hgdprs5030835
ensemblrs5030835
gopubmedrs5030835
geneviewrs5030835
scholarrs5030835
googlers5030835
pharmgkbrs5030835
gwascentralrs5030835
openSNPrs5030835
23andMers5030835
23andMe allrs5030835
SNP Nexus

SNPshotrs5030835
SNPdbers5030835
MSV3drs5030835
GWAS Ctlgrs5030835
Max Magnitude0
ClinVar
Risk rs5030835(G;G)
Alt rs5030835(G;G)
Reference rs5030835(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene VHL
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.10191532C>G
CLNSRC
CLNACC RCV000161082.1,