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rs587783007

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587783007(-;-)
Make rs587783007(-;T)
Make rs587783007(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position15645228
GeneBTD
is asnp
is mentioned by
dbSNPrs587783007
ebirs587783007
HLIrs587783007
Exacrs587783007
Varsomers587783007
Maprs587783007
PheGenIrs587783007
hapmaprs587783007
1000 genomesrs587783007
hgdprs587783007
ensemblrs587783007
gopubmedrs587783007
geneviewrs587783007
scholarrs587783007
googlers587783007
pharmgkbrs587783007
gwascentralrs587783007
openSNPrs587783007
23andMers587783007
23andMe allrs587783007
SNP Nexus

SNPshotrs587783007
SNPdbers587783007
MSV3drs587783007
GWAS Ctlgrs587783007
Max Magnitude0
ClinVar
Risk rs587783007(T;T)
Alt rs587783007(T;T)
Reference rs587783007(;)
Significance Pathogenic
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15686735dupT
CLNSRC
CLNACC RCV000144062.1,