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rs869025630

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025630(G;T)
Make rs869025630(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10142158
GeneVHL
is asnp
is mentioned by
dbSNPrs869025630
ebirs869025630
HLIrs869025630
Exacrs869025630
Varsomers869025630
Maprs869025630
PheGenIrs869025630
hapmaprs869025630
1000 genomesrs869025630
hgdprs869025630
ensemblrs869025630
gopubmedrs869025630
geneviewrs869025630
scholarrs869025630
googlers869025630
pharmgkbrs869025630
gwascentralrs869025630
openSNPrs869025630
23andMers869025630
23andMe allrs869025630
SNP Nexus

SNPshotrs869025630
SNPdbers869025630
MSV3drs869025630
GWAS Ctlgrs869025630
Max Magnitude0
ClinVar
Risk rs869025630(T;T)
Alt rs869025630(T;T)
Reference rs869025630(G;G)
Significance Probable-Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183842G>T
CLNSRC
CLNACC RCV000208803.1,