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rs869025668

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025668(G;T)
Make rs869025668(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10149964
GeneVHL
is asnp
is mentioned by
dbSNPrs869025668
ebirs869025668
HLIrs869025668
Exacrs869025668
Varsomers869025668
Maprs869025668
PheGenIrs869025668
hapmaprs869025668
1000 genomesrs869025668
hgdprs869025668
ensemblrs869025668
gopubmedrs869025668
geneviewrs869025668
scholarrs869025668
googlers869025668
pharmgkbrs869025668
gwascentralrs869025668
openSNPrs869025668
23andMers869025668
23andMe allrs869025668
SNP Nexus

SNPshotrs869025668
SNPdbers869025668
MSV3drs869025668
GWAS Ctlgrs869025668
Max Magnitude0
ClinVar
Risk rs869025668(T;T)
Alt rs869025668(T;T)
Reference rs869025668(G;G)
Significance Probable-Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10191648G>T
CLNSRC
CLNACC RCV000208844.1,