Have questions? Visit https://www.reddit.com/r/SNPedia

rs869025667

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025667(C;C)
Make rs869025667(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10149916
GeneVHL
is asnp
is mentioned by
dbSNPrs869025667
ebirs869025667
HLIrs869025667
Exacrs869025667
Varsomers869025667
Maprs869025667
PheGenIrs869025667
hapmaprs869025667
1000 genomesrs869025667
hgdprs869025667
ensemblrs869025667
gopubmedrs869025667
geneviewrs869025667
scholarrs869025667
googlers869025667
pharmgkbrs869025667
gwascentralrs869025667
openSNPrs869025667
23andMers869025667
23andMe allrs869025667
SNP Nexus

SNPshotrs869025667
SNPdbers869025667
MSV3drs869025667
GWAS Ctlgrs869025667
Max Magnitude0
ClinVar
Risk rs869025667(C;C)
Alt rs869025667(C;C)
Reference rs869025667(T;T)
Significance Probable-Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10191600T>C
CLNSRC
CLNACC RCV000208871.1,