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rs374681173

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs374681173(A;G)
Make rs374681173(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position15642052
GeneBTD
is asnp
is mentioned by
dbSNPrs374681173
ebirs374681173
HLIrs374681173
Exacrs374681173
Varsomers374681173
Maprs374681173
PheGenIrs374681173
hapmaprs374681173
1000 genomesrs374681173
hgdprs374681173
ensemblrs374681173
gopubmedrs374681173
geneviewrs374681173
scholarrs374681173
googlers374681173
pharmgkbrs374681173
gwascentralrs374681173
openSNPrs374681173
23andMers374681173
23andMe allrs374681173
SNP Nexus

SNPshotrs374681173
SNPdbers374681173
MSV3drs374681173
GWAS Ctlgrs374681173
Max Magnitude0
ClinVar
Risk rs374681173(C,G;C,G)
Alt rs374681173(C,G;C,G)
Reference rs374681173(A;A)
Significance Pathogenic
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15683559A>C
CLNSRC ARUP BTD
CLNACC RCV000021927.1,