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rs2239907

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2239907(A;G)
Make rs2239907(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position28398728
GeneSARM1, SLC46A1
is asnp
is mentioned by
dbSNPrs2239907
dbSNP (old)rs2239907
ClinGenrs2239907
ebirs2239907
HLIrs2239907
Exacrs2239907
Gnomadrs2239907
Varsomers2239907
Maprs2239907
PheGenIrs2239907
Biobankrs2239907
1000 genomesrs2239907
hgdprs2239907
ensemblrs2239907
gopubmedrs2239907
geneviewrs2239907
scholarrs2239907
googlers2239907
pharmgkbrs2239907
gwascentralrs2239907
openSNPrs2239907
23andMers2239907
23andMe allrs2239907
SNP Nexus

SNPshotrs2239907
SNPdbers2239907
MSV3drs2239907
GWAS Ctlgrs2239907
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 25124723] SLC19A1, SLC46A1 and SLCO1B1 Polymorphisms As Predictors Of Methotrexate-Related Toxicity In Portuguese Rheumatoid Arthritis Patients


ClinVar
Risk rs2239907(G;G)
Alt rs2239907(G;G)
Reference Rs2239907(A;A)
Significance Non-pathogenic
Disease Congenital defect of folate absorption
Variation info
Gene SLC46A1 SARM1
CLNDBN Congenital defect of folate absorption
Reversed 1
HGVS NC_000017.10:g.26725744T>C
CLNSRC
CLNACC RCV000387903.1,