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rs869025640

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025640(-;-)
Make rs869025640(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10146524
GeneVHL
is asnp
is mentioned by
dbSNPrs869025640
ebirs869025640
HLIrs869025640
Exacrs869025640
Varsomers869025640
Maprs869025640
PheGenIrs869025640
hapmaprs869025640
1000 genomesrs869025640
hgdprs869025640
ensemblrs869025640
gopubmedrs869025640
geneviewrs869025640
scholarrs869025640
googlers869025640
pharmgkbrs869025640
gwascentralrs869025640
openSNPrs869025640
23andMers869025640
23andMe allrs869025640
SNP Nexus

SNPshotrs869025640
SNPdbers869025640
MSV3drs869025640
GWAS Ctlgrs869025640
Max Magnitude0
ClinVar
Risk rs869025640(;)
Alt rs869025640(;)
Reference rs869025640(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.10188208delG
CLNSRC
CLNACC RCV000208786.1,