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rs397514366

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397514366(A;G)
Make rs397514366(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position15644371
GeneBTD
is asnp
is mentioned by
dbSNPrs397514366
ebirs397514366
HLIrs397514366
Exacrs397514366
Varsomers397514366
Maprs397514366
PheGenIrs397514366
hapmaprs397514366
1000 genomesrs397514366
hgdprs397514366
ensemblrs397514366
gopubmedrs397514366
geneviewrs397514366
scholarrs397514366
googlers397514366
pharmgkbrs397514366
gwascentralrs397514366
openSNPrs397514366
23andMers397514366
23andMe allrs397514366
SNP Nexus

SNPshotrs397514366
SNPdbers397514366
MSV3drs397514366
GWAS Ctlgrs397514366
Max Magnitude0
ClinVar
Risk rs397514366(G;G)
Alt rs397514366(G;G)
Reference rs397514366(A;A)
Significance Pathogenic
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15685878A>G
CLNSRC ARUP BTD
CLNACC RCV000021937.1,