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rs397514370

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397514370(A;G)
Make rs397514370(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position15644439
GeneBTD
is asnp
is mentioned by
dbSNPrs397514370
ebirs397514370
HLIrs397514370
Exacrs397514370
Varsomers397514370
Maprs397514370
PheGenIrs397514370
hapmaprs397514370
1000 genomesrs397514370
hgdprs397514370
ensemblrs397514370
gopubmedrs397514370
geneviewrs397514370
scholarrs397514370
googlers397514370
pharmgkbrs397514370
gwascentralrs397514370
openSNPrs397514370
23andMers397514370
23andMe allrs397514370
SNP Nexus

SNPshotrs397514370
SNPdbers397514370
MSV3drs397514370
GWAS Ctlgrs397514370
Max Magnitude0
ClinVar
Risk rs397514370(G;G)
Alt rs397514370(G;G)
Reference rs397514370(A;A)
Significance Pathogenic
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15685946A>G
CLNSRC ARUP BTD
CLNACC RCV000021942.1,