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rs397515573

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515573(-;-)
Make rs397515573(-;G)
Make rs397515573(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position28405920
GeneSLC46A1
is asnp
is mentioned by
dbSNPrs397515573
ebirs397515573
HLIrs397515573
Exacrs397515573
Varsomers397515573
Maprs397515573
PheGenIrs397515573
hapmaprs397515573
1000 genomesrs397515573
hgdprs397515573
ensemblrs397515573
gopubmedrs397515573
geneviewrs397515573
scholarrs397515573
googlers397515573
pharmgkbrs397515573
gwascentralrs397515573
openSNPrs397515573
23andMers397515573
23andMe allrs397515573
SNP Nexus

SNPshotrs397515573
SNPdbers397515573
MSV3drs397515573
GWAS Ctlgrs397515573
Max Magnitude0
ClinVar
Risk rs397515573(G;G)
Alt rs397515573(G;G)
Reference rs397515573(;)
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.26732939dupC
CLNSRC ClinVar GeneReviews
CLNACC RCV000055981.1,