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rs397507175

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507175(A;A)
Make rs397507175(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position15644590
GeneBTD
is asnp
is mentioned by
dbSNPrs397507175
ebirs397507175
HLIrs397507175
Exacrs397507175
Varsomers397507175
Maprs397507175
PheGenIrs397507175
hapmaprs397507175
1000 genomesrs397507175
hgdprs397507175
ensemblrs397507175
gopubmedrs397507175
geneviewrs397507175
scholarrs397507175
googlers397507175
pharmgkbrs397507175
gwascentralrs397507175
openSNPrs397507175
23andMers397507175
23andMe allrs397507175
SNP Nexus

SNPshotrs397507175
SNPdbers397507175
MSV3drs397507175
GWAS Ctlgrs397507175
Max Magnitude0
ClinVar
Risk rs397507175(A;A)
Alt rs397507175(A;A)
Reference rs397507175(G;G)
Significance Other
Disease Biotinidase deficiency
Variation info
Gene BTD
CLNDBN Biotinidase deficiency
Reversed 0
HGVS NC_000003.11:g.15686097G>A
CLNSRC ARUP BTD
CLNACC RCV000021959.2,