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rs397514369

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514369(A;A)
Make rs397514369(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position15644413
GeneBTD
is asnp
is mentioned by
dbSNPrs397514369
ebirs397514369
HLIrs397514369
Exacrs397514369
Varsomers397514369
Maprs397514369
PheGenIrs397514369
hapmaprs397514369
1000 genomesrs397514369
hgdprs397514369
ensemblrs397514369
gopubmedrs397514369
geneviewrs397514369
scholarrs397514369
googlers397514369
pharmgkbrs397514369
gwascentralrs397514369
openSNPrs397514369
23andMers397514369
23andMe allrs397514369
SNP Nexus

SNPshotrs397514369
SNPdbers397514369
MSV3drs397514369
GWAS Ctlgrs397514369
Max Magnitude0
ClinVar
Risk rs397514369(A;A)
Alt rs397514369(A;A)
Reference rs397514369(G;G)
Significance Other
Disease Biotinidase deficiency not provided
Variation info
Gene BTD
CLNDBN Biotinidase deficiency not provided
Reversed 0
HGVS NC_000003.11:g.15685920G>A
CLNSRC ARUP BTD HGMD
CLNACC RCV000021940.2, RCV000078075.3,