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rs587780732

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587780732(C;G)
Make rs587780732(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position10146589
GeneVHL
is asnp
is mentioned by
dbSNPrs587780732
ebirs587780732
HLIrs587780732
Exacrs587780732
Varsomers587780732
Maprs587780732
PheGenIrs587780732
hapmaprs587780732
1000 genomesrs587780732
hgdprs587780732
ensemblrs587780732
gopubmedrs587780732
geneviewrs587780732
scholarrs587780732
googlers587780732
pharmgkbrs587780732
gwascentralrs587780732
openSNPrs587780732
23andMers587780732
23andMe allrs587780732
SNP Nexus

SNPshotrs587780732
SNPdbers587780732
MSV3drs587780732
GWAS Ctlgrs587780732
Max Magnitude0
ClinVar
Risk rs587780732(G,T;G,T)
Alt rs587780732(G,T;G,T)
Reference rs587780732(C;C)
Significance Probable-Pathogenic
Disease Von Hippel-Lindau syndrome not specified
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome not specified
Reversed 0
HGVS NC_000003.11:g.10188273C>G; NC_000003.11:g.10188273C>T
CLNSRC
CLNACC RCV000123107.1, RCV000161079.2, RCV000196415.1,