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rs730882033

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730882033(C;C)
Make rs730882033(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position10142074
GeneVHL
is asnp
is mentioned by
dbSNPrs730882033
ebirs730882033
HLIrs730882033
Exacrs730882033
Varsomers730882033
Maprs730882033
PheGenIrs730882033
hapmaprs730882033
1000 genomesrs730882033
hgdprs730882033
ensemblrs730882033
gopubmedrs730882033
geneviewrs730882033
scholarrs730882033
googlers730882033
pharmgkbrs730882033
gwascentralrs730882033
openSNPrs730882033
23andMers730882033
23andMe allrs730882033
SNP Nexus

SNPshotrs730882033
SNPdbers730882033
MSV3drs730882033
GWAS Ctlgrs730882033
Max Magnitude0
ClinVar
Risk rs730882033(C;C)
Alt rs730882033(C;C)
Reference rs730882033(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene VHL
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.10183758T>C
CLNSRC
CLNACC RCV000161084.1,