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rs869025649

From SNPedia

Orientationplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs869025649(-;-)
Make rs869025649(-;TC)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10146592
GeneVHL
is asnp
is mentioned by
dbSNPrs869025649
ebirs869025649
HLIrs869025649
Exacrs869025649
Varsomers869025649
Maprs869025649
PheGenIrs869025649
hapmaprs869025649
1000 genomesrs869025649
hgdprs869025649
ensemblrs869025649
gopubmedrs869025649
geneviewrs869025649
scholarrs869025649
googlers869025649
pharmgkbrs869025649
gwascentralrs869025649
openSNPrs869025649
23andMers869025649
23andMe allrs869025649
SNP Nexus

SNPshotrs869025649
SNPdbers869025649
MSV3drs869025649
GWAS Ctlgrs869025649
Max Magnitude0
ClinVar
Risk rs869025649(;)
Alt rs869025649(;)
Reference rs869025649(TC;TC)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10188276_10188277delTC
CLNSRC
CLNACC RCV000208805.1,