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rs869025638

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025638(-;-)
Make rs869025638(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10146514
GeneVHL
is asnp
is mentioned by
dbSNPrs869025638
ebirs869025638
HLIrs869025638
Exacrs869025638
Varsomers869025638
Maprs869025638
PheGenIrs869025638
hapmaprs869025638
1000 genomesrs869025638
hgdprs869025638
ensemblrs869025638
gopubmedrs869025638
geneviewrs869025638
scholarrs869025638
googlers869025638
pharmgkbrs869025638
gwascentralrs869025638
openSNPrs869025638
23andMers869025638
23andMe allrs869025638
SNP Nexus

SNPshotrs869025638
SNPdbers869025638
MSV3drs869025638
GWAS Ctlgrs869025638
Max Magnitude0
ClinVar
Risk rs869025638(;)
Alt rs869025638(;)
Reference rs869025638(G;G)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10188198delG
CLNSRC
CLNACC RCV000208824.1,