Have questions? Visit https://www.reddit.com/r/SNPedia

rs587783002

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783002(G;G)
Make rs587783002(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position15635636
GeneBTD
is asnp
is mentioned by
dbSNPrs587783002
ebirs587783002
HLIrs587783002
Exacrs587783002
Varsomers587783002
Maprs587783002
PheGenIrs587783002
hapmaprs587783002
1000 genomesrs587783002
hgdprs587783002
ensemblrs587783002
gopubmedrs587783002
geneviewrs587783002
scholarrs587783002
googlers587783002
pharmgkbrs587783002
gwascentralrs587783002
openSNPrs587783002
23andMers587783002
23andMe allrs587783002
SNP Nexus

SNPshotrs587783002
SNPdbers587783002
MSV3drs587783002
GWAS Ctlgrs587783002
Max Magnitude0
ClinVar
Risk rs587783002(G;G)
Alt rs587783002(G;G)
Reference rs587783002(T;T)
Significance Pathogenic
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15677143T>G
CLNSRC
CLNACC RCV000144056.1,