rs2239907

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs2239907(A;G)

Make rs2239907(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

28398728

Gene	SARM1, SLC46A1

is a	snp
is	mentioned by
dbSNP	rs2239907
dbSNP (classic)	rs2239907
ClinGen	rs2239907
ebi	rs2239907
HLI	rs2239907
Exac	rs2239907
Gnomad	rs2239907
Varsome	rs2239907
LitVar	rs2239907
Map	rs2239907
PheGenI	rs2239907
Biobank	rs2239907
1000 genomes	rs2239907
hgdp	rs2239907
ensembl	rs2239907
geneview	rs2239907
scholar	rs2239907
google	rs2239907
pharmgkb	rs2239907
gwascentral	rs2239907
openSNP	rs2239907
23andMe	rs2239907
SNPshot	rs2239907
SNPdbe	rs2239907
MSV3d	rs2239907
GWAS Ctlg	rs2239907

Max Magnitude

0

?	(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,