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rs397514355

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397514355(G;G)
Make rs397514355(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position15641980
GeneBTD
is asnp
is mentioned by
dbSNPrs397514355
ebirs397514355
HLIrs397514355
Exacrs397514355
Varsomers397514355
Maprs397514355
PheGenIrs397514355
hapmaprs397514355
1000 genomesrs397514355
hgdprs397514355
ensemblrs397514355
gopubmedrs397514355
geneviewrs397514355
scholarrs397514355
googlers397514355
pharmgkbrs397514355
gwascentralrs397514355
openSNPrs397514355
23andMers397514355
23andMe allrs397514355
SNP Nexus

SNPshotrs397514355
SNPdbers397514355
MSV3drs397514355
GWAS Ctlgrs397514355
Max Magnitude0
ClinVar
Risk rs397514355(G;G)
Alt rs397514355(G;G)
Reference rs397514355(T;T)
Significance Pathogenic
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15683487T>G
CLNSRC ARUP BTD
CLNACC RCV000021921.1,