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

rs397514411

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397514411(-;-)
Make rs397514411(-;C)
Make rs397514411(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position15645120
GeneBTD
is asnp
is mentioned by
dbSNPrs397514411
ebirs397514411
HLIrs397514411
Exacrs397514411
Varsomers397514411
Maprs397514411
PheGenIrs397514411
hapmaprs397514411
1000 genomesrs397514411
hgdprs397514411
ensemblrs397514411
gopubmedrs397514411
geneviewrs397514411
scholarrs397514411
googlers397514411
pharmgkbrs397514411
gwascentralrs397514411
openSNPrs397514411
23andMers397514411
23andMe allrs397514411
SNP Nexus

SNPshotrs397514411
SNPdbers397514411
MSV3drs397514411
GWAS Ctlgrs397514411
Max Magnitude0
ClinVar
Risk rs397514411(C;C)
Alt rs397514411(C;C)
Reference rs397514411(;)
Significance Pathogenic
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15686627dupC
CLNSRC ClinVar
CLNACC RCV000021997.1,