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rs869025644

From SNPedia

Orientationplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs869025644(-;-)
Make rs869025644(-;AC)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10146547
GeneVHL
is asnp
is mentioned by
dbSNPrs869025644
ebirs869025644
HLIrs869025644
Exacrs869025644
Varsomers869025644
Maprs869025644
PheGenIrs869025644
hapmaprs869025644
1000 genomesrs869025644
hgdprs869025644
ensemblrs869025644
gopubmedrs869025644
geneviewrs869025644
scholarrs869025644
googlers869025644
pharmgkbrs869025644
gwascentralrs869025644
openSNPrs869025644
23andMers869025644
23andMe allrs869025644
SNP Nexus

SNPshotrs869025644
SNPdbers869025644
MSV3drs869025644
GWAS Ctlgrs869025644
Max Magnitude0
ClinVar
Risk rs869025644(;)
Alt rs869025644(;)
Reference rs869025644(AC;AC)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10188231_10188232delAC
CLNSRC
CLNACC RCV000208802.1,