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rs397514398

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514398(-;-)
Make rs397514398(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position15644908
GeneBTD
is asnp
is mentioned by
dbSNPrs397514398
ebirs397514398
HLIrs397514398
Exacrs397514398
Varsomers397514398
Maprs397514398
PheGenIrs397514398
hapmaprs397514398
1000 genomesrs397514398
hgdprs397514398
ensemblrs397514398
gopubmedrs397514398
geneviewrs397514398
scholarrs397514398
googlers397514398
pharmgkbrs397514398
gwascentralrs397514398
openSNPrs397514398
23andMers397514398
23andMe allrs397514398
SNP Nexus

SNPshotrs397514398
SNPdbers397514398
MSV3drs397514398
GWAS Ctlgrs397514398
Max Magnitude0
ClinVar
Risk rs397514398(;)
Alt rs397514398(;)
Reference rs397514398(C;C)
Significance Pathogenic
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15686415delC
CLNSRC ClinVar
CLNACC RCV000021980.1,