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rs730882032

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730882032(C;C)
Make rs730882032(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position10142188
GeneVHL
is asnp
is mentioned by
dbSNPrs730882032
ebirs730882032
HLIrs730882032
Exacrs730882032
Varsomers730882032
Maprs730882032
PheGenIrs730882032
hapmaprs730882032
1000 genomesrs730882032
hgdprs730882032
ensemblrs730882032
gopubmedrs730882032
geneviewrs730882032
scholarrs730882032
googlers730882032
pharmgkbrs730882032
gwascentralrs730882032
openSNPrs730882032
23andMers730882032
23andMe allrs730882032
SNP Nexus

SNPshotrs730882032
SNPdbers730882032
MSV3drs730882032
GWAS Ctlgrs730882032
Max Magnitude0
ClinVar
Risk rs730882032(C;C)
Alt rs730882032(C;C)
Reference rs730882032(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.10183872G>A; NC_000003.11:g.10183872G>C
CLNSRC
CLNACC RCV000208808.1, RCV000161078.1,