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rs869025660

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869025660(C;T)
Make rs869025660(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10149793
GeneVHL
is asnp
is mentioned by
dbSNPrs869025660
ebirs869025660
HLIrs869025660
Exacrs869025660
Varsomers869025660
Maprs869025660
PheGenIrs869025660
hapmaprs869025660
1000 genomesrs869025660
hgdprs869025660
ensemblrs869025660
gopubmedrs869025660
geneviewrs869025660
scholarrs869025660
googlers869025660
pharmgkbrs869025660
gwascentralrs869025660
openSNPrs869025660
23andMers869025660
23andMe allrs869025660
SNP Nexus

SNPshotrs869025660
SNPdbers869025660
MSV3drs869025660
GWAS Ctlgrs869025660
Max Magnitude0
ClinVar
Risk rs869025660(T;T)
Alt rs869025660(T;T)
Reference rs869025660(C;C)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10191477C>T
CLNSRC
CLNACC RCV000208862.1,