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

rs137853122

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853122(G;G)
Make rs137853122(G;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position37084339
GeneTMPRSS6
is asnp
is mentioned by
dbSNPrs137853122
ebirs137853122
HLIrs137853122
Exacrs137853122
Varsomers137853122
Maprs137853122
PheGenIrs137853122
hapmaprs137853122
1000 genomesrs137853122
hgdprs137853122
ensemblrs137853122
gopubmedrs137853122
geneviewrs137853122
scholarrs137853122
googlers137853122
pharmgkbrs137853122
gwascentralrs137853122
openSNPrs137853122
23andMers137853122
23andMe allrs137853122
SNP Nexus

SNPshotrs137853122
SNPdbers137853122
MSV3drs137853122
GWAS Ctlgrs137853122
Max Magnitude0
OMIM609862
Desc
Variant0009
Relatedalso
ClinVar
Risk rs137853122(G;G)
Alt rs137853122(G;G)
Reference rs137853122(T;T)
Significance Pathogenic
Disease Microcytic anemia
Variation info
Gene TMPRSS6
CLNDBN Microcytic anemia
Reversed 1
HGVS NC_000022.10:g.37480379A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001472.4,