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rs398123481

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123481(C;G)
Make rs398123481(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position10142103
GeneVHL
is asnp
is mentioned by
dbSNPrs398123481
ebirs398123481
HLIrs398123481
Exacrs398123481
Varsomers398123481
Maprs398123481
PheGenIrs398123481
hapmaprs398123481
1000 genomesrs398123481
hgdprs398123481
ensemblrs398123481
gopubmedrs398123481
geneviewrs398123481
scholarrs398123481
googlers398123481
pharmgkbrs398123481
gwascentralrs398123481
openSNPrs398123481
23andMers398123481
23andMe allrs398123481
SNP Nexus

SNPshotrs398123481
SNPdbers398123481
MSV3drs398123481
GWAS Ctlgrs398123481
Max Magnitude0
ClinVar
Risk rs398123481(G,T;G,T)
Alt rs398123481(G,T;G,T)
Reference rs398123481(C;C)
Significance Other
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183787C>G; NC_000003.11:g.10183787C>T
CLNSRC HGMD
CLNACC RCV000079208.5, RCV000155449.2,