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rs146136265

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146136265(A;A)
Make rs146136265(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position15645485
GeneBTD
is asnp
is mentioned by
dbSNPrs146136265
ebirs146136265
HLIrs146136265
Exacrs146136265
Varsomers146136265
Maprs146136265
PheGenIrs146136265
hapmaprs146136265
1000 genomesrs146136265
hgdprs146136265
ensemblrs146136265
gopubmedrs146136265
geneviewrs146136265
scholarrs146136265
googlers146136265
pharmgkbrs146136265
gwascentralrs146136265
openSNPrs146136265
23andMers146136265
23andMe allrs146136265
SNP Nexus

SNPshotrs146136265
SNPdbers146136265
MSV3drs146136265
GWAS Ctlgrs146136265
Max Magnitude0
ClinVar
Risk rs146136265(A;A)
Alt rs146136265(A;A)
Reference rs146136265(C;C)
Significance Probable-Pathogenic
Disease Biotinidase deficiency not provided
Variation info
Gene BTD
CLNDBN Biotinidase deficiency not provided
Reversed 0
HGVS NC_000003.11:g.15686992C>A
CLNSRC ARUP BTD
CLNACC RCV000022028.1, RCV000078071.4,