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rs587783004

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783004(A;G)
Make rs587783004(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position15644539
GeneBTD
is asnp
is mentioned by
dbSNPrs587783004
ebirs587783004
HLIrs587783004
Exacrs587783004
Varsomers587783004
Maprs587783004
PheGenIrs587783004
hapmaprs587783004
1000 genomesrs587783004
hgdprs587783004
ensemblrs587783004
gopubmedrs587783004
geneviewrs587783004
scholarrs587783004
googlers587783004
pharmgkbrs587783004
gwascentralrs587783004
openSNPrs587783004
23andMers587783004
23andMe allrs587783004
SNP Nexus

SNPshotrs587783004
SNPdbers587783004
MSV3drs587783004
GWAS Ctlgrs587783004
Max Magnitude0
ClinVar
Risk rs587783004(G;G)
Alt rs587783004(G;G)
Reference rs587783004(A;A)
Significance Pathogenic
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15686046A>G
CLNSRC
CLNACC RCV000144059.1,