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rs200337373

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200337373(A;A)
Make rs200337373(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position15644520
GeneBTD
is asnp
is mentioned by
dbSNPrs200337373
ebirs200337373
HLIrs200337373
Exacrs200337373
Varsomers200337373
Maprs200337373
PheGenIrs200337373
hapmaprs200337373
1000 genomesrs200337373
hgdprs200337373
ensemblrs200337373
gopubmedrs200337373
geneviewrs200337373
scholarrs200337373
googlers200337373
pharmgkbrs200337373
gwascentralrs200337373
openSNPrs200337373
23andMers200337373
23andMe allrs200337373
SNP Nexus

SNPshotrs200337373
SNPdbers200337373
MSV3drs200337373
GWAS Ctlgrs200337373
Max Magnitude0
ClinVar
Risk rs200337373(A,C;A,C)
Alt rs200337373(A,C;A,C)
Reference rs200337373(G;G)
Significance Pathogenic
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15686027G>C
CLNSRC ARUP BTD
CLNACC RCV000022031.1,