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rs151071780

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151071780(C;G)
Make rs151071780(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position15635641
GeneBTD
is asnp
is mentioned by
dbSNPrs151071780
ebirs151071780
HLIrs151071780
Exacrs151071780
Varsomers151071780
Maprs151071780
PheGenIrs151071780
hapmaprs151071780
1000 genomesrs151071780
hgdprs151071780
ensemblrs151071780
gopubmedrs151071780
geneviewrs151071780
scholarrs151071780
googlers151071780
pharmgkbrs151071780
gwascentralrs151071780
openSNPrs151071780
23andMers151071780
23andMe allrs151071780
SNP Nexus

SNPshotrs151071780
SNPdbers151071780
MSV3drs151071780
GWAS Ctlgrs151071780
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs151071780(G,T;G,T)
Alt rs151071780(G,T;G,T)
Reference rs151071780(C;C)
Significance Pathogenic
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15677148C>T
CLNSRC ARUP BTD
CLNACC RCV000021910.1,