Have questions? Visit https://www.reddit.com/r/SNPedia

rs121918331

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918331(C;C)
Make rs121918331(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position39391956
GeneSLC25A38
is asnp
is mentioned by
dbSNPrs121918331
ebirs121918331
HLIrs121918331
Exacrs121918331
Varsomers121918331
Maprs121918331
PheGenIrs121918331
hapmaprs121918331
1000 genomesrs121918331
hgdprs121918331
ensemblrs121918331
gopubmedrs121918331
geneviewrs121918331
scholarrs121918331
googlers121918331
pharmgkbrs121918331
gwascentralrs121918331
openSNPrs121918331
23andMers121918331
23andMe allrs121918331
SNP Nexus

SNPshotrs121918331
SNPdbers121918331
MSV3drs121918331
GWAS Ctlgrs121918331
Max Magnitude0
OMIM610819
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121918331(C;C)
Alt rs121918331(C;C)
Reference rs121918331(G;G)
Significance Pathogenic
Disease Anemia
Variation info
Gene SLC25A38
CLNDBN Anemia, sideroblastic, pyridoxine-refractory, autosomal recessive
Reversed 0
HGVS NC_000003.11:g.39433447G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001179.3,