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rs869025625

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025625(-;-)
Make rs869025625(-;C)
Make rs869025625(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10142143
GeneVHL
is asnp
is mentioned by
dbSNPrs869025625
ebirs869025625
HLIrs869025625
Exacrs869025625
Varsomers869025625
Maprs869025625
PheGenIrs869025625
hapmaprs869025625
1000 genomesrs869025625
hgdprs869025625
ensemblrs869025625
gopubmedrs869025625
geneviewrs869025625
scholarrs869025625
googlers869025625
pharmgkbrs869025625
gwascentralrs869025625
openSNPrs869025625
23andMers869025625
23andMe allrs869025625
SNP Nexus

SNPshotrs869025625
SNPdbers869025625
MSV3drs869025625
GWAS Ctlgrs869025625
Max Magnitude0
ClinVar
Risk rs869025625(C;C)
Alt rs869025625(C;C)
Reference rs869025625(;)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183827dupC
CLNSRC
CLNACC RCV000208817.1,