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rs869025627

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025627(-;-)
Make rs869025627(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10142156
GeneVHL
is asnp
is mentioned by
dbSNPrs869025627
ebirs869025627
HLIrs869025627
Exacrs869025627
Varsomers869025627
Maprs869025627
PheGenIrs869025627
hapmaprs869025627
1000 genomesrs869025627
hgdprs869025627
ensemblrs869025627
gopubmedrs869025627
geneviewrs869025627
scholarrs869025627
googlers869025627
pharmgkbrs869025627
gwascentralrs869025627
openSNPrs869025627
23andMers869025627
23andMe allrs869025627
SNP Nexus

SNPshotrs869025627
SNPdbers869025627
MSV3drs869025627
GWAS Ctlgrs869025627
Max Magnitude0
ClinVar
Risk rs869025627(;)
Alt rs869025627(;)
Reference rs869025627(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.10183840delT
CLNSRC
CLNACC RCV000208801.1,