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rs367902696

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 3 Carrier of a biotinidase deficiency mutation
(G;G) 0 common in clinvar


Make rs367902696(A;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position15642041
GeneBTD
is asnp
is mentioned by
dbSNPrs367902696
dbSNP (classic)rs367902696
ClinGenrs367902696
ebirs367902696
HLIrs367902696
Exacrs367902696
Gnomadrs367902696
Varsomers367902696
LitVarrs367902696
Maprs367902696
PheGenIrs367902696
Biobankrs367902696
1000 genomesrs367902696
hgdprs367902696
ensemblrs367902696
geneviewrs367902696
scholarrs367902696
googlers367902696
pharmgkbrs367902696
gwascentralrs367902696
openSNPrs367902696
23andMers367902696
SNPshotrs367902696
SNPdbers367902696
MSV3drs367902696
GWAS Ctlgrs367902696
Max Magnitude3
ClinVar
Risk rs367902696(A;A)
Alt rs367902696(A;A)
Reference Rs367902696(G;G)
Significance Pathogenic
Disease Biotinidase deficiency not provided
Variation info
Gene BTD
CLNDBN Biotinidase deficiency not provided
Reversed 0
HGVS NC_000003.11:g.15683548G>A
CLNSRC ARUP BTD
CLNACC RCV000021924.1, RCV000490188.1,