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rs869025620

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025620(-;-)
Make rs869025620(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10142068
GeneVHL
is asnp
is mentioned by
dbSNPrs869025620
ebirs869025620
HLIrs869025620
Exacrs869025620
Varsomers869025620
Maprs869025620
PheGenIrs869025620
hapmaprs869025620
1000 genomesrs869025620
hgdprs869025620
ensemblrs869025620
gopubmedrs869025620
geneviewrs869025620
scholarrs869025620
googlers869025620
pharmgkbrs869025620
gwascentralrs869025620
openSNPrs869025620
23andMers869025620
23andMe allrs869025620
SNP Nexus

SNPshotrs869025620
SNPdbers869025620
MSV3drs869025620
GWAS Ctlgrs869025620
Max Magnitude0
ClinVar
Risk rs869025620(;)
Alt rs869025620(;)
Reference rs869025620(T;T)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183752delT
CLNSRC
CLNACC RCV000208849.1,