Have questions? Visit https://www.reddit.com/r/SNPedia

rs397514428

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514428(A;A)
Make rs397514428(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position15645466
GeneBTD
is asnp
is mentioned by
dbSNPrs397514428
ebirs397514428
HLIrs397514428
Exacrs397514428
Varsomers397514428
Maprs397514428
PheGenIrs397514428
hapmaprs397514428
1000 genomesrs397514428
hgdprs397514428
ensemblrs397514428
gopubmedrs397514428
geneviewrs397514428
scholarrs397514428
googlers397514428
pharmgkbrs397514428
gwascentralrs397514428
openSNPrs397514428
23andMers397514428
23andMe allrs397514428
SNP Nexus

SNPshotrs397514428
SNPdbers397514428
MSV3drs397514428
GWAS Ctlgrs397514428
Max Magnitude0
ClinVar
Risk rs397514428(A;A)
Alt rs397514428(A;A)
Reference rs397514428(G;G)
Significance Pathogenic
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15686973G>A
CLNSRC ARUP BTD
CLNACC RCV000022023.1,