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rs587780077

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780077(G;T)
Make rs587780077(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position10146618
GeneVHL
is asnp
is mentioned by
dbSNPrs587780077
ebirs587780077
HLIrs587780077
Exacrs587780077
Varsomers587780077
Maprs587780077
PheGenIrs587780077
hapmaprs587780077
1000 genomesrs587780077
hgdprs587780077
ensemblrs587780077
gopubmedrs587780077
geneviewrs587780077
scholarrs587780077
googlers587780077
pharmgkbrs587780077
gwascentralrs587780077
openSNPrs587780077
23andMers587780077
23andMe allrs587780077
SNP Nexus

SNPshotrs587780077
SNPdbers587780077
MSV3drs587780077
GWAS Ctlgrs587780077
Max Magnitude0
ClinVar
Risk rs587780077(A,C,T;A,C,T)
Alt rs587780077(A,C,T;A,C,T)
Reference rs587780077(G;G)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome not provided
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome not provided
Reversed 0
HGVS NC_000003.11:g.10188302G>A; NC_000003.11:g.10188302G>C; NC_000003.11:g.10188302G>T
CLNSRC
CLNACC RCV000208822.1, RCV000208855.1, RCV000115746.3, RCV000208783.1,