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rs869025624

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025624(-;-)
Make rs869025624(-;A)
Make rs869025624(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10142140
GeneVHL
is asnp
is mentioned by
dbSNPrs869025624
ebirs869025624
HLIrs869025624
Exacrs869025624
Varsomers869025624
Maprs869025624
PheGenIrs869025624
hapmaprs869025624
1000 genomesrs869025624
hgdprs869025624
ensemblrs869025624
gopubmedrs869025624
geneviewrs869025624
scholarrs869025624
googlers869025624
pharmgkbrs869025624
gwascentralrs869025624
openSNPrs869025624
23andMers869025624
23andMe allrs869025624
SNP Nexus

SNPshotrs869025624
SNPdbers869025624
MSV3drs869025624
GWAS Ctlgrs869025624
Max Magnitude0
ClinVar
Risk rs869025624(A;A)
Alt rs869025624(A;A)
Reference rs869025624(;)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183824dupA
CLNSRC
CLNACC RCV000208788.1,