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rs869025642

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025642(A;G)
Make rs869025642(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10146531
GeneVHL
is asnp
is mentioned by
dbSNPrs869025642
ebirs869025642
HLIrs869025642
Exacrs869025642
Varsomers869025642
Maprs869025642
PheGenIrs869025642
hapmaprs869025642
1000 genomesrs869025642
hgdprs869025642
ensemblrs869025642
gopubmedrs869025642
geneviewrs869025642
scholarrs869025642
googlers869025642
pharmgkbrs869025642
gwascentralrs869025642
openSNPrs869025642
23andMers869025642
23andMe allrs869025642
SNP Nexus

SNPshotrs869025642
SNPdbers869025642
MSV3drs869025642
GWAS Ctlgrs869025642
Max Magnitude0
ClinVar
Risk rs869025642(G;G)
Alt rs869025642(G;G)
Reference rs869025642(A;A)
Significance Probable-Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10188215A>G
CLNSRC
CLNACC RCV000208800.1,