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rs730882030

From SNPedia

Orientationplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs730882030(-;-)
Make rs730882030(-;GC)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position10149937
GeneVHL
is asnp
is mentioned by
dbSNPrs730882030
ebirs730882030
HLIrs730882030
Exacrs730882030
Varsomers730882030
Maprs730882030
PheGenIrs730882030
hapmaprs730882030
1000 genomesrs730882030
hgdprs730882030
ensemblrs730882030
gopubmedrs730882030
geneviewrs730882030
scholarrs730882030
googlers730882030
pharmgkbrs730882030
gwascentralrs730882030
openSNPrs730882030
23andMers730882030
23andMe allrs730882030
SNP Nexus

SNPshotrs730882030
SNPdbers730882030
MSV3drs730882030
GWAS Ctlgrs730882030
Max Magnitude0
ClinVar
Risk rs730882030(;)
Alt rs730882030(;)
Reference rs730882030(GC;GC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene VHL
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000003.11:g.10191621_10191622delGC
CLNSRC
CLNACC RCV000161075.1,