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

rs397514336

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514336(G;T)
Make rs397514336(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position15635515
GeneBTD
is asnp
is mentioned by
dbSNPrs397514336
ebirs397514336
HLIrs397514336
Exacrs397514336
Varsomers397514336
Maprs397514336
PheGenIrs397514336
hapmaprs397514336
1000 genomesrs397514336
hgdprs397514336
ensemblrs397514336
gopubmedrs397514336
geneviewrs397514336
scholarrs397514336
googlers397514336
pharmgkbrs397514336
gwascentralrs397514336
openSNPrs397514336
23andMers397514336
23andMe allrs397514336
SNP Nexus

SNPshotrs397514336
SNPdbers397514336
MSV3drs397514336
GWAS Ctlgrs397514336
Max Magnitude0
ClinVar
Risk rs397514336(T;T)
Alt rs397514336(T;T)
Reference rs397514336(G;G)
Significance Pathogenic
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15677022G>T
CLNSRC ARUP BTD
CLNACC RCV000021891.1,