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rs397515574

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515574(-;-)
Make rs397515574(-;C)
Make rs397515574(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position28406091
GeneSLC46A1
is asnp
is mentioned by
dbSNPrs397515574
ebirs397515574
HLIrs397515574
Exacrs397515574
Varsomers397515574
Maprs397515574
PheGenIrs397515574
hapmaprs397515574
1000 genomesrs397515574
hgdprs397515574
ensemblrs397515574
gopubmedrs397515574
geneviewrs397515574
scholarrs397515574
googlers397515574
pharmgkbrs397515574
gwascentralrs397515574
openSNPrs397515574
23andMers397515574
23andMe allrs397515574
SNP Nexus

SNPshotrs397515574
SNPdbers397515574
MSV3drs397515574
GWAS Ctlgrs397515574
Max Magnitude0
ClinVar
Risk rs397515574(C;C)
Alt rs397515574(C;C)
Reference rs397515574(;)
Significance Pathogenic
Disease Congenital defect of folate absorption
Variation info
Gene SLC46A1
CLNDBN Congenital defect of folate absorption
Reversed 1
HGVS NC_000017.10:g.26733110dupG
CLNSRC ClinVar GeneReviews
CLNACC RCV000055983.1,