rs281875211

Orientation

minus

Stabilized

minus

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

Make rs281875211(A;A)

Make rs281875211(A;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

28402276

Gene

SLC46A1

is a	snp
is	mentioned by
dbSNP	rs281875211
dbSNP (classic)	rs281875211
ClinGen	rs281875211
ebi	rs281875211
HLI	rs281875211
Exac	rs281875211
Gnomad	rs281875211
Varsome	rs281875211
LitVar	rs281875211
Map	rs281875211
PheGenI	rs281875211
Biobank	rs281875211
1000 genomes	rs281875211
hgdp	rs281875211
ensembl	rs281875211
geneview	rs281875211
scholar	rs281875211
google	rs281875211
pharmgkb	rs281875211
gwascentral	rs281875211
openSNP	rs281875211
23andMe	rs281875211
SNPshot	rs281875211
SNPdbe	rs281875211
MSV3d	rs281875211
GWAS Ctlg	rs281875211

Max Magnitude

0

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 (protein) UniProtKB (variants)
CLNACC	RCV000055980.1, RCV000059711.1,