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rs786205059

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205059(C;C)
Make rs786205059(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position37069072
GeneTMPRSS6
is asnp
is mentioned by
dbSNPrs786205059
ebirs786205059
HLIrs786205059
Exacrs786205059
Varsomers786205059
Maprs786205059
PheGenIrs786205059
hapmaprs786205059
1000 genomesrs786205059
hgdprs786205059
ensemblrs786205059
gopubmedrs786205059
geneviewrs786205059
scholarrs786205059
googlers786205059
pharmgkbrs786205059
gwascentralrs786205059
openSNPrs786205059
23andMers786205059
23andMe allrs786205059
SNP Nexus

SNPshotrs786205059
SNPdbers786205059
MSV3drs786205059
GWAS Ctlgrs786205059
Max Magnitude0
ClinVar
Risk rs786205059(C;C)
Alt rs786205059(C;C)
Reference rs786205059(G;G)
Significance Pathogenic
Disease Microcytic anemia
Variation info
Gene TMPRSS6
CLNDBN Microcytic anemia
Reversed 1
HGVS NC_000022.10:g.37465112C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001467.4,