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rs869025645

From SNPedia

Orientationplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs869025645(GC;TT)
Make rs869025645(TT;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10146554
GeneVHL
is asnp
is mentioned by
dbSNPrs869025645
ebirs869025645
HLIrs869025645
Exacrs869025645
Varsomers869025645
Maprs869025645
PheGenIrs869025645
hapmaprs869025645
1000 genomesrs869025645
hgdprs869025645
ensemblrs869025645
gopubmedrs869025645
geneviewrs869025645
scholarrs869025645
googlers869025645
pharmgkbrs869025645
gwascentralrs869025645
openSNPrs869025645
23andMers869025645
23andMe allrs869025645
SNP Nexus

SNPshotrs869025645
SNPdbers869025645
MSV3drs869025645
GWAS Ctlgrs869025645
Max Magnitude0
ClinVar
Risk rs869025645(TT;TT)
Alt rs869025645(TT;TT)
Reference rs869025645(GC;GC)
Significance Probable-Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10188238_10188239delGCinsTT
CLNSRC
CLNACC RCV000208832.1,