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rs869025650

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025650(G;T)
Make rs869025650(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10146603
GeneVHL
is asnp
is mentioned by
dbSNPrs869025650
ebirs869025650
HLIrs869025650
Exacrs869025650
Varsomers869025650
Maprs869025650
PheGenIrs869025650
hapmaprs869025650
1000 genomesrs869025650
hgdprs869025650
ensemblrs869025650
gopubmedrs869025650
geneviewrs869025650
scholarrs869025650
googlers869025650
pharmgkbrs869025650
gwascentralrs869025650
openSNPrs869025650
23andMers869025650
23andMe allrs869025650
SNP Nexus

SNPshotrs869025650
SNPdbers869025650
MSV3drs869025650
GWAS Ctlgrs869025650
Max Magnitude0
ClinVar
Risk rs869025650(T;T)
Alt rs869025650(T;T)
Reference rs869025650(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.10188287G>T
CLNSRC
CLNACC RCV000208850.1,