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rs869320724

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869320724(-;-)
Make rs869320724(-;GC)
Make rs869320724(GC;GC)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position37069307
GeneTMPRSS6
is asnp
is mentioned by
dbSNPrs869320724
ebirs869320724
HLIrs869320724
Exacrs869320724
Varsomers869320724
Maprs869320724
PheGenIrs869320724
hapmaprs869320724
1000 genomesrs869320724
hgdprs869320724
ensemblrs869320724
gopubmedrs869320724
geneviewrs869320724
scholarrs869320724
googlers869320724
pharmgkbrs869320724
gwascentralrs869320724
openSNPrs869320724
23andMers869320724
23andMe allrs869320724
SNP Nexus

SNPshotrs869320724
SNPdbers869320724
MSV3drs869320724
GWAS Ctlgrs869320724
Max Magnitude0
ClinVar
Risk rs869320724(GC;GC)
Alt rs869320724(GC;GC)
Reference rs869320724(;)
Significance Pathogenic
Disease Microcytic anemia
Variation info
Gene TMPRSS6
CLNDBN Microcytic anemia
Reversed 1
HGVS NC_000022.10:g.37465348_37465349dupGC
CLNSRC OMIM Allelic Variant
CLNACC RCV000001464.3,