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rs267607121

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607121(A;A)
Make rs267607121(A;C)
ReferenceGRCh38 38.1/141
Chromosome22
Position37098426
GeneTMPRSS6
is asnp
is mentioned by
dbSNPrs267607121
ebirs267607121
HLIrs267607121
Exacrs267607121
Varsomers267607121
Maprs267607121
PheGenIrs267607121
hapmaprs267607121
1000 genomesrs267607121
hgdprs267607121
ensemblrs267607121
gopubmedrs267607121
geneviewrs267607121
scholarrs267607121
googlers267607121
pharmgkbrs267607121
gwascentralrs267607121
openSNPrs267607121
23andMers267607121
23andMe allrs267607121
SNP Nexus

SNPshotrs267607121
SNPdbers267607121
MSV3drs267607121
GWAS Ctlgrs267607121
Max Magnitude0
ClinVar
Risk rs267607121(A;A)
Alt rs267607121(A;A)
Reference rs267607121(C;C)
Significance Pathogenic
Disease Microcytic anemia
Variation info
Gene TMPRSS6
CLNDBN Microcytic anemia
Reversed 1
HGVS NC_000022.10:g.37494466G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001475.3,