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rs367902696

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs367902696(A;A)
Make rs367902696(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position15642041
GeneBTD
is asnp
is mentioned by
dbSNPrs367902696
ebirs367902696
HLIrs367902696
Exacrs367902696
Varsomers367902696
Maprs367902696
PheGenIrs367902696
hapmaprs367902696
1000 genomesrs367902696
hgdprs367902696
ensemblrs367902696
gopubmedrs367902696
geneviewrs367902696
scholarrs367902696
googlers367902696
pharmgkbrs367902696
gwascentralrs367902696
openSNPrs367902696
23andMers367902696
23andMe allrs367902696
SNP Nexus

SNPshotrs367902696
SNPdbers367902696
MSV3drs367902696
GWAS Ctlgrs367902696
Max Magnitude0
ClinVar
Risk rs367902696(A;A)
Alt rs367902696(A;A)
Reference rs367902696(G;G)
Significance Pathogenic
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15683548G>A
CLNSRC ARUP BTD
CLNACC RCV000021924.1,