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rs869025653

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025653(-;-)
Make rs869025653(-;T)
Make rs869025653(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10146617
GeneVHL
is asnp
is mentioned by
dbSNPrs869025653
ebirs869025653
HLIrs869025653
Exacrs869025653
Varsomers869025653
Maprs869025653
PheGenIrs869025653
hapmaprs869025653
1000 genomesrs869025653
hgdprs869025653
ensemblrs869025653
gopubmedrs869025653
geneviewrs869025653
scholarrs869025653
googlers869025653
pharmgkbrs869025653
gwascentralrs869025653
openSNPrs869025653
23andMers869025653
23andMe allrs869025653
SNP Nexus

SNPshotrs869025653
SNPdbers869025653
MSV3drs869025653
GWAS Ctlgrs869025653
Max Magnitude0
ClinVar
Risk rs869025653(T;T)
Alt rs869025653(T;T)
Reference rs869025653(;)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10188301dupT
CLNSRC
CLNACC RCV000208839.1,