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rs398123139

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123139(A;A)
Make rs398123139(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position15644482
GeneBTD
is asnp
is mentioned by
dbSNPrs398123139
ebirs398123139
HLIrs398123139
Exacrs398123139
Varsomers398123139
Maprs398123139
PheGenIrs398123139
hapmaprs398123139
1000 genomesrs398123139
hgdprs398123139
ensemblrs398123139
gopubmedrs398123139
geneviewrs398123139
scholarrs398123139
googlers398123139
pharmgkbrs398123139
gwascentralrs398123139
openSNPrs398123139
23andMers398123139
23andMe allrs398123139
SNP Nexus

SNPshotrs398123139
SNPdbers398123139
MSV3drs398123139
GWAS Ctlgrs398123139
Max Magnitude0
ClinVar
Risk rs398123139(A;A)
Alt rs398123139(A;A)
Reference rs398123139(G;G)
Significance Pathogenic
Disease not provided Biotinidase deficiency not specified
Variation info
Gene BTD
CLNDBN not provided Biotinidase deficiency not specified
Reversed 0
HGVS NC_000003.11:g.15685989G>A
CLNSRC ClinVar Emory University
CLNACC RCV000078076.4, RCV000144058.1, RCV000185803.1,