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rs869025622

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025622(G;T)
Make rs869025622(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10142111
GeneVHL
is asnp
is mentioned by
dbSNPrs869025622
ebirs869025622
HLIrs869025622
Exacrs869025622
Varsomers869025622
Maprs869025622
PheGenIrs869025622
hapmaprs869025622
1000 genomesrs869025622
hgdprs869025622
ensemblrs869025622
gopubmedrs869025622
geneviewrs869025622
scholarrs869025622
googlers869025622
pharmgkbrs869025622
gwascentralrs869025622
openSNPrs869025622
23andMers869025622
23andMe allrs869025622
SNP Nexus

SNPshotrs869025622
SNPdbers869025622
MSV3drs869025622
GWAS Ctlgrs869025622
Max Magnitude0
ClinVar
Risk rs869025622(T;T)
Alt rs869025622(T;T)
Reference rs869025622(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.10183795G>T
CLNSRC
CLNACC RCV000208827.1,