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rs730882039

From SNPedia

Orientationplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs730882039(-;-)
Make rs730882039(-;GG)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position10142066
GeneVHL
is asnp
is mentioned by
dbSNPrs730882039
ebirs730882039
HLIrs730882039
Exacrs730882039
Varsomers730882039
Maprs730882039
PheGenIrs730882039
hapmaprs730882039
1000 genomesrs730882039
hgdprs730882039
ensemblrs730882039
gopubmedrs730882039
geneviewrs730882039
scholarrs730882039
googlers730882039
pharmgkbrs730882039
gwascentralrs730882039
openSNPrs730882039
23andMers730882039
23andMe allrs730882039
SNP Nexus

SNPshotrs730882039
SNPdbers730882039
MSV3drs730882039
GWAS Ctlgrs730882039
Max Magnitude0
ClinVar
Risk rs730882039(;)
Alt rs730882039(;)
Reference rs730882039(GG;GG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene VHL
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.10183750_10183751delGG
CLNSRC
CLNACC RCV000161098.1,