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rs869025637

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025637(A;G)
Make rs869025637(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10146512
GeneVHL
is asnp
is mentioned by
dbSNPrs869025637
ebirs869025637
HLIrs869025637
Exacrs869025637
Varsomers869025637
Maprs869025637
PheGenIrs869025637
hapmaprs869025637
1000 genomesrs869025637
hgdprs869025637
ensemblrs869025637
gopubmedrs869025637
geneviewrs869025637
scholarrs869025637
googlers869025637
pharmgkbrs869025637
gwascentralrs869025637
openSNPrs869025637
23andMers869025637
23andMe allrs869025637
SNP Nexus

SNPshotrs869025637
SNPdbers869025637
MSV3drs869025637
GWAS Ctlgrs869025637
Max Magnitude0
ClinVar
Risk rs869025637(G;G)
Alt rs869025637(G;G)
Reference rs869025637(A;A)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10188196A>G
CLNSRC
CLNACC RCV000208784.1,