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rs869025628

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025628(-;-)
Make rs869025628(-;T)
Make rs869025628(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10142156
GeneVHL
is asnp
is mentioned by
dbSNPrs869025628
ebirs869025628
HLIrs869025628
Exacrs869025628
Varsomers869025628
Maprs869025628
PheGenIrs869025628
hapmaprs869025628
1000 genomesrs869025628
hgdprs869025628
ensemblrs869025628
gopubmedrs869025628
geneviewrs869025628
scholarrs869025628
googlers869025628
pharmgkbrs869025628
gwascentralrs869025628
openSNPrs869025628
23andMers869025628
23andMe allrs869025628
SNP Nexus

SNPshotrs869025628
SNPdbers869025628
MSV3drs869025628
GWAS Ctlgrs869025628
Max Magnitude0
ClinVar
Risk rs869025628(T;T)
Alt rs869025628(T;T)
Reference rs869025628(;)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183840dupT
CLNSRC
CLNACC RCV000208819.1,