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rs137853119

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853119(A;A)
Make rs137853119(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position37075180
GeneTMPRSS6
is asnp
is mentioned by
dbSNPrs137853119
ebirs137853119
HLIrs137853119
Exacrs137853119
Varsomers137853119
Maprs137853119
PheGenIrs137853119
hapmaprs137853119
1000 genomesrs137853119
hgdprs137853119
ensemblrs137853119
gopubmedrs137853119
geneviewrs137853119
scholarrs137853119
googlers137853119
pharmgkbrs137853119
gwascentralrs137853119
openSNPrs137853119
23andMers137853119
23andMe allrs137853119
SNP Nexus

SNPshotrs137853119
SNPdbers137853119
MSV3drs137853119
GWAS Ctlgrs137853119
Max Magnitude0
OMIM609862
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137853119(A;A)
Alt rs137853119(A;A)
Reference rs137853119(G;G)
Significance Pathogenic
Disease Microcytic anemia
Variation info
Gene TMPRSS6
CLNDBN Microcytic anemia
Reversed 1
HGVS NC_000022.10:g.37471220C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001468.2,