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rs267607202

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607202(A;T)
Make rs267607202(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position12885368
GeneKLF1
is asnp
is mentioned by
dbSNPrs267607202
ebirs267607202
HLIrs267607202
Exacrs267607202
Varsomers267607202
Maprs267607202
PheGenIrs267607202
hapmaprs267607202
1000 genomesrs267607202
hgdprs267607202
ensemblrs267607202
gopubmedrs267607202
geneviewrs267607202
scholarrs267607202
googlers267607202
pharmgkbrs267607202
gwascentralrs267607202
openSNPrs267607202
23andMers267607202
23andMe allrs267607202
SNP Nexus

SNPshotrs267607202
SNPdbers267607202
MSV3drs267607202
GWAS Ctlgrs267607202
Max Magnitude0
ClinVar
Risk rs267607202(T;T)
Alt rs267607202(T;T)
Reference rs267607202(A;A)
Significance Pathogenic
Disease HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN
Variation info
Gene KLF1
CLNDBN HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN, KLF1-RELATED
Reversed 1
HGVS NC_000019.9:g.12996182T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009566.4,