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rs730882031

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730882031(-;-)
Make rs730882031(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position10142039
GeneVHL
is asnp
is mentioned by
dbSNPrs730882031
ebirs730882031
HLIrs730882031
Exacrs730882031
Varsomers730882031
Maprs730882031
PheGenIrs730882031
hapmaprs730882031
1000 genomesrs730882031
hgdprs730882031
ensemblrs730882031
gopubmedrs730882031
geneviewrs730882031
scholarrs730882031
googlers730882031
pharmgkbrs730882031
gwascentralrs730882031
openSNPrs730882031
23andMers730882031
23andMe allrs730882031
SNP Nexus

SNPshotrs730882031
SNPdbers730882031
MSV3drs730882031
GWAS Ctlgrs730882031
Max Magnitude0
ClinVar
Risk rs730882031(;)
Alt rs730882031(;)
Reference rs730882031(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.10183723delC
CLNSRC
CLNACC RCV000161076.1,