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rs281875211

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281875211(A;A)
Make rs281875211(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position28402276
GeneSLC46A1
is asnp
is mentioned by
dbSNPrs281875211
ebirs281875211
HLIrs281875211
Exacrs281875211
Varsomers281875211
Maprs281875211
PheGenIrs281875211
hapmaprs281875211
1000 genomesrs281875211
hgdprs281875211
ensemblrs281875211
gopubmedrs281875211
geneviewrs281875211
scholarrs281875211
googlers281875211
pharmgkbrs281875211
gwascentralrs281875211
openSNPrs281875211
23andMers281875211
23andMe allrs281875211
SNP Nexus

SNPshotrs281875211
SNPdbers281875211
MSV3drs281875211
GWAS Ctlgrs281875211
Max Magnitude0
ClinVar
Risk rs281875211(A;A)
Alt rs281875211(A;A)
Reference rs281875211(G;G)
Significance Pathogenic
Disease Congenital defect of folate absorption not provided
Variation info
Gene SLC46A1
CLNDBN Congenital defect of folate absorption not provided
Reversed 1
HGVS NC_000017.10:g.26729294C>T
CLNSRC UniProtKB (variants)
CLNACC RCV000055980.1, RCV000059711.1,