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rs869025636

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025636(C;C)
Make rs869025636(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10142187
GeneVHL
is asnp
is mentioned by
dbSNPrs869025636
ebirs869025636
HLIrs869025636
Exacrs869025636
Varsomers869025636
Maprs869025636
PheGenIrs869025636
hapmaprs869025636
1000 genomesrs869025636
hgdprs869025636
ensemblrs869025636
gopubmedrs869025636
geneviewrs869025636
scholarrs869025636
googlers869025636
pharmgkbrs869025636
gwascentralrs869025636
openSNPrs869025636
23andMers869025636
23andMe allrs869025636
SNP Nexus

SNPshotrs869025636
SNPdbers869025636
MSV3drs869025636
GWAS Ctlgrs869025636
Max Magnitude0
ClinVar
Risk rs869025636(C;C)
Alt rs869025636(C;C)
Reference rs869025636(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.10183871G>C
CLNSRC
CLNACC RCV000208843.1,