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rs397507174

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507174(A;G)
Make rs397507174(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position15644485
GeneBTD
is asnp
is mentioned by
dbSNPrs397507174
ebirs397507174
HLIrs397507174
Exacrs397507174
Varsomers397507174
Maprs397507174
PheGenIrs397507174
hapmaprs397507174
1000 genomesrs397507174
hgdprs397507174
ensemblrs397507174
gopubmedrs397507174
geneviewrs397507174
scholarrs397507174
googlers397507174
pharmgkbrs397507174
gwascentralrs397507174
openSNPrs397507174
23andMers397507174
23andMe allrs397507174
SNP Nexus

SNPshotrs397507174
SNPdbers397507174
MSV3drs397507174
GWAS Ctlgrs397507174
Max Magnitude0
ClinVar
Risk rs397507174(G;G)
Alt rs397507174(G;G)
Reference rs397507174(A;A)
Significance Other
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15685992A>G
CLNSRC ARUP ARUP BTD
CLNACC RCV000021949.2,