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rs387907598

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907598(C;C)
Make rs387907598(C;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position12885338
GeneKLF1
is asnp
is mentioned by
dbSNPrs387907598
ebirs387907598
HLIrs387907598
Exacrs387907598
Varsomers387907598
Maprs387907598
PheGenIrs387907598
hapmaprs387907598
1000 genomesrs387907598
hgdprs387907598
ensemblrs387907598
gopubmedrs387907598
geneviewrs387907598
scholarrs387907598
googlers387907598
pharmgkbrs387907598
gwascentralrs387907598
openSNPrs387907598
23andMers387907598
23andMe allrs387907598
SNP Nexus

SNPshotrs387907598
SNPdbers387907598
MSV3drs387907598
GWAS Ctlgrs387907598
Max Magnitude0
ClinVar
Risk rs387907598(C;C)
Alt rs387907598(C;C)
Reference rs387907598(G;G)
Significance Pathogenic
Disease BLOOD GROUP--LUTHERAN INHIBITOR Congenital dyserythropoietic anemia Fetal hemoglobin quantitative trait locus 6
Variation info
Gene KLF1
CLNDBN BLOOD GROUP--LUTHERAN INHIBITOR Congenital dyserythropoietic anemia, type IV Fetal hemoglobin quantitative trait locus 6
Reversed 1
HGVS NC_000019.9:g.12996152C>G
CLNSRC ClinVar
CLNACC RCV000050236.1,