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rs137853120

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853120(A;A)
Make rs137853120(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position37073553
GeneTMPRSS6
is asnp
is mentioned by
dbSNPrs137853120
ebirs137853120
HLIrs137853120
Exacrs137853120
Varsomers137853120
Maprs137853120
PheGenIrs137853120
hapmaprs137853120
1000 genomesrs137853120
hgdprs137853120
ensemblrs137853120
gopubmedrs137853120
geneviewrs137853120
scholarrs137853120
googlers137853120
pharmgkbrs137853120
gwascentralrs137853120
openSNPrs137853120
23andMers137853120
23andMe allrs137853120
SNP Nexus

SNPshotrs137853120
SNPdbers137853120
MSV3drs137853120
GWAS Ctlgrs137853120
GMAF0.0004591
Max Magnitude0
OMIM609862
Desc
Variant0006
Relatedalso
ClinVar
Risk rs137853120(A;A)
Alt rs137853120(A;A)
Reference rs137853120(G;G)
Significance Pathogenic
Disease Microcytic anemia
Variation info
Gene TMPRSS6
CLNDBN Microcytic anemia
Reversed 1
HGVS NC_000022.10:g.37469593C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001469.4,