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rs137853123

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853123(C;T)
Make rs137853123(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position37070557
GeneTMPRSS6
is asnp
is mentioned by
dbSNPrs137853123
ebirs137853123
HLIrs137853123
Exacrs137853123
Varsomers137853123
Maprs137853123
PheGenIrs137853123
hapmaprs137853123
1000 genomesrs137853123
hgdprs137853123
ensemblrs137853123
gopubmedrs137853123
geneviewrs137853123
scholarrs137853123
googlers137853123
pharmgkbrs137853123
gwascentralrs137853123
openSNPrs137853123
23andMers137853123
23andMe allrs137853123
SNP Nexus

SNPshotrs137853123
SNPdbers137853123
MSV3drs137853123
GWAS Ctlgrs137853123
Max Magnitude0
OMIM609862
Desc
Variant0010
Relatedalso
ClinVar
Risk rs137853123(T;T)
Alt rs137853123(T;T)
Reference rs137853123(C;C)
Significance Pathogenic
Disease Microcytic anemia
Variation info
Gene TMPRSS6
CLNDBN Microcytic anemia
Reversed 1
HGVS NC_000022.10:g.37466597G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001473.3,