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rs869025616

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025616(G;G)
Make rs869025616(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10142040
GeneVHL
is asnp
is mentioned by
dbSNPrs869025616
ebirs869025616
HLIrs869025616
Exacrs869025616
Varsomers869025616
Maprs869025616
PheGenIrs869025616
hapmaprs869025616
1000 genomesrs869025616
hgdprs869025616
ensemblrs869025616
gopubmedrs869025616
geneviewrs869025616
scholarrs869025616
googlers869025616
pharmgkbrs869025616
gwascentralrs869025616
openSNPrs869025616
23andMers869025616
23andMe allrs869025616
SNP Nexus

SNPshotrs869025616
SNPdbers869025616
MSV3drs869025616
GWAS Ctlgrs869025616
Max Magnitude0
ClinVar
Risk rs869025616(G;G)
Alt rs869025616(G;G)
Reference rs869025616(T;T)
Significance Probable-Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183724T>G
CLNSRC
CLNACC RCV000208812.1,