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rs869025654

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025654(-;-)
Make rs869025654(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10146617
GeneVHL
is asnp
is mentioned by
dbSNPrs869025654
ebirs869025654
HLIrs869025654
Exacrs869025654
Varsomers869025654
Maprs869025654
PheGenIrs869025654
hapmaprs869025654
1000 genomesrs869025654
hgdprs869025654
ensemblrs869025654
gopubmedrs869025654
geneviewrs869025654
scholarrs869025654
googlers869025654
pharmgkbrs869025654
gwascentralrs869025654
openSNPrs869025654
23andMers869025654
23andMe allrs869025654
SNP Nexus

SNPshotrs869025654
SNPdbers869025654
MSV3drs869025654
GWAS Ctlgrs869025654
Max Magnitude0
ClinVar
Risk rs869025654(;)
Alt rs869025654(;)
Reference rs869025654(T;T)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10188301delT
CLNSRC
CLNACC RCV000208793.1,