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rs869025626

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025626(-;-)
Make rs869025626(-;G)
Make rs869025626(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10142147
GeneVHL
is asnp
is mentioned by
dbSNPrs869025626
ebirs869025626
HLIrs869025626
Exacrs869025626
Varsomers869025626
Maprs869025626
PheGenIrs869025626
hapmaprs869025626
1000 genomesrs869025626
hgdprs869025626
ensemblrs869025626
gopubmedrs869025626
geneviewrs869025626
scholarrs869025626
googlers869025626
pharmgkbrs869025626
gwascentralrs869025626
openSNPrs869025626
23andMers869025626
23andMe allrs869025626
SNP Nexus

SNPshotrs869025626
SNPdbers869025626
MSV3drs869025626
GWAS Ctlgrs869025626
Max Magnitude0
ClinVar
Risk rs869025626(G;G)
Alt rs869025626(G;G)
Reference rs869025626(;)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183831dupG
CLNSRC
CLNACC RCV000208859.1,