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rs137853121

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853121(A;A)
Make rs137853121(A;C)
ReferenceGRCh38 38.1/141
Chromosome22
Position37084775
GeneTMPRSS6
is asnp
is mentioned by
dbSNPrs137853121
ebirs137853121
HLIrs137853121
Exacrs137853121
Varsomers137853121
Maprs137853121
PheGenIrs137853121
hapmaprs137853121
1000 genomesrs137853121
hgdprs137853121
ensemblrs137853121
gopubmedrs137853121
geneviewrs137853121
scholarrs137853121
googlers137853121
pharmgkbrs137853121
gwascentralrs137853121
openSNPrs137853121
23andMers137853121
23andMe allrs137853121
SNP Nexus

SNPshotrs137853121
SNPdbers137853121
MSV3drs137853121
GWAS Ctlgrs137853121
GMAF0.0009183
Max Magnitude0
OMIM609862
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137853121(A;A)
Alt rs137853121(A;A)
Reference rs137853121(C;C)
Significance Pathogenic
Disease Microcytic anemia
Variation info
Gene TMPRSS6
CLNDBN Microcytic anemia
Reversed 1
HGVS NC_000022.10:g.37480815G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001470.3,