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rs397514377

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397514377(A;G)
Make rs397514377(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position15644497
GeneBTD
is asnp
is mentioned by
dbSNPrs397514377
ebirs397514377
HLIrs397514377
Exacrs397514377
Varsomers397514377
Maprs397514377
PheGenIrs397514377
hapmaprs397514377
1000 genomesrs397514377
hgdprs397514377
ensemblrs397514377
gopubmedrs397514377
geneviewrs397514377
scholarrs397514377
googlers397514377
pharmgkbrs397514377
gwascentralrs397514377
openSNPrs397514377
23andMers397514377
23andMe allrs397514377
SNP Nexus

SNPshotrs397514377
SNPdbers397514377
MSV3drs397514377
GWAS Ctlgrs397514377
Max Magnitude0
ClinVar
Risk rs397514377(G;G)
Alt rs397514377(G;G)
Reference rs397514377(A;A)
Significance Pathogenic
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15686004A>G
CLNSRC ARUP BTD
CLNACC RCV000021952.1, RCV000032022.1,