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rs35976361

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs35976361(A;G)
Make rs35976361(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position15644736
GeneBTD
is asnp
is mentioned by
dbSNPrs35976361
ebirs35976361
HLIrs35976361
Exacrs35976361
Varsomers35976361
Maprs35976361
PheGenIrs35976361
hapmaprs35976361
1000 genomesrs35976361
hgdprs35976361
ensemblrs35976361
gopubmedrs35976361
geneviewrs35976361
scholarrs35976361
googlers35976361
pharmgkbrs35976361
gwascentralrs35976361
openSNPrs35976361
23andMers35976361
23andMe allrs35976361
SNP Nexus

SNPshotrs35976361
SNPdbers35976361
MSV3drs35976361
GWAS Ctlgrs35976361
GMAF0.01148
Max Magnitude0
ClinVar
Risk rs35976361(G;G)
Alt rs35976361(G;G)
Reference rs35976361(A;A)
Significance Pathogenic
Disease Biotinidase deficiency not provided
Variation info
Gene BTD
CLNDBN Biotinidase deficiency not provided
Reversed 0
HGVS NC_000003.11:g.15686243A>G
CLNSRC ARUP BTD
CLNACC RCV000021969.1, RCV000224487.1,