Have questions? Visit https://www.reddit.com/r/SNPedia

rs869025646

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025646(-;-)
Make rs869025646(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10146575
GeneVHL
is asnp
is mentioned by
dbSNPrs869025646
ebirs869025646
HLIrs869025646
Exacrs869025646
Varsomers869025646
Maprs869025646
PheGenIrs869025646
hapmaprs869025646
1000 genomesrs869025646
hgdprs869025646
ensemblrs869025646
gopubmedrs869025646
geneviewrs869025646
scholarrs869025646
googlers869025646
pharmgkbrs869025646
gwascentralrs869025646
openSNPrs869025646
23andMers869025646
23andMe allrs869025646
SNP Nexus

SNPshotrs869025646
SNPdbers869025646
MSV3drs869025646
GWAS Ctlgrs869025646
Max Magnitude0
ClinVar
Risk rs869025646(;)
Alt rs869025646(;)
Reference rs869025646(A;A)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10188259delA
CLNSRC
CLNACC RCV000208816.1,