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rs397515391

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs397515391(-;-)
Make rs397515391(-;CC)
ReferenceGRCh38 38.1/141
Chromosome17
Position28405910
GeneSLC46A1
is asnp
is mentioned by
dbSNPrs397515391
ebirs397515391
HLIrs397515391
Exacrs397515391
Varsomers397515391
Maprs397515391
PheGenIrs397515391
hapmaprs397515391
1000 genomesrs397515391
hgdprs397515391
ensemblrs397515391
gopubmedrs397515391
geneviewrs397515391
scholarrs397515391
googlers397515391
pharmgkbrs397515391
gwascentralrs397515391
openSNPrs397515391
23andMers397515391
23andMe allrs397515391
SNP Nexus

SNPshotrs397515391
SNPdbers397515391
MSV3drs397515391
GWAS Ctlgrs397515391
Max Magnitude0
ClinVar
Risk rs397515391(;)
Alt rs397515391(;)
Reference rs397515391(CC;CC)
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.26732928_26732929delGG
CLNSRC OMIM Allelic Variant
CLNACC RCV000023912.5,