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rs730882020

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730882020(-;-)
Make rs730882020(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position10149800
GeneVHL
is asnp
is mentioned by
dbSNPrs730882020
ebirs730882020
HLIrs730882020
Exacrs730882020
Varsomers730882020
Maprs730882020
PheGenIrs730882020
hapmaprs730882020
1000 genomesrs730882020
hgdprs730882020
ensemblrs730882020
gopubmedrs730882020
geneviewrs730882020
scholarrs730882020
googlers730882020
pharmgkbrs730882020
gwascentralrs730882020
openSNPrs730882020
23andMers730882020
23andMe allrs730882020
SNP Nexus

SNPshotrs730882020
SNPdbers730882020
MSV3drs730882020
GWAS Ctlgrs730882020
Max Magnitude0
ClinVar
Risk rs730882020(;)
Alt rs730882020(;)
Reference rs730882020(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Hereditary cancer-predisposing syndrome Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10191484delA
CLNSRC
CLNACC RCV000161061.1, RCV000208863.1,