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rs869025623

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025623(-;-)
Make rs869025623(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10142116
GeneVHL
is asnp
is mentioned by
dbSNPrs869025623
ebirs869025623
HLIrs869025623
Exacrs869025623
Varsomers869025623
Maprs869025623
PheGenIrs869025623
hapmaprs869025623
1000 genomesrs869025623
hgdprs869025623
ensemblrs869025623
gopubmedrs869025623
geneviewrs869025623
scholarrs869025623
googlers869025623
pharmgkbrs869025623
gwascentralrs869025623
openSNPrs869025623
23andMers869025623
23andMe allrs869025623
SNP Nexus

SNPshotrs869025623
SNPdbers869025623
MSV3drs869025623
GWAS Ctlgrs869025623
Max Magnitude0
ClinVar
Risk rs869025623(;)
Alt rs869025623(;)
Reference rs869025623(A;A)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183800delA
CLNSRC
CLNACC RCV000208842.1,