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rs786205057

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205057(-;-)
Make rs786205057(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position37070539
GeneTMPRSS6
is asnp
is mentioned by
dbSNPrs786205057
ebirs786205057
HLIrs786205057
Exacrs786205057
Varsomers786205057
Maprs786205057
PheGenIrs786205057
hapmaprs786205057
1000 genomesrs786205057
hgdprs786205057
ensemblrs786205057
gopubmedrs786205057
geneviewrs786205057
scholarrs786205057
googlers786205057
pharmgkbrs786205057
gwascentralrs786205057
openSNPrs786205057
23andMers786205057
23andMe allrs786205057
SNP Nexus

SNPshotrs786205057
SNPdbers786205057
MSV3drs786205057
GWAS Ctlgrs786205057
Max Magnitude0
ClinVar
Risk rs786205057(;)
Alt rs786205057(;)
Reference rs786205057(G;G)
Significance Pathogenic
Disease Microcytic anemia
Variation info
Gene TMPRSS6
CLNDBN Microcytic anemia
Reversed 1
HGVS NC_000022.10:g.37466579delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000001465.4,