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rs730882034

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730882034(C;T)
Make rs730882034(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position10142104
GeneVHL
is asnp
is mentioned by
dbSNPrs730882034
ebirs730882034
HLIrs730882034
Exacrs730882034
Varsomers730882034
Maprs730882034
PheGenIrs730882034
hapmaprs730882034
1000 genomesrs730882034
hgdprs730882034
ensemblrs730882034
gopubmedrs730882034
geneviewrs730882034
scholarrs730882034
googlers730882034
pharmgkbrs730882034
gwascentralrs730882034
openSNPrs730882034
23andMers730882034
23andMe allrs730882034
SNP Nexus

SNPshotrs730882034
SNPdbers730882034
MSV3drs730882034
GWAS Ctlgrs730882034
Max Magnitude0
ClinVar
Risk rs730882034(T;T)
Alt rs730882034(T;T)
Reference rs730882034(C;C)
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.10183788C>G; NC_000003.11:g.10183788C>T
CLNSRC
CLNACC RCV000208868.1, RCV000161085.1, RCV000208836.1,