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rs786205058

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205058(A;A)
Make rs786205058(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position37073531
GeneTMPRSS6
is asnp
is mentioned by
dbSNPrs786205058
ebirs786205058
HLIrs786205058
Exacrs786205058
Varsomers786205058
Maprs786205058
PheGenIrs786205058
hapmaprs786205058
1000 genomesrs786205058
hgdprs786205058
ensemblrs786205058
gopubmedrs786205058
geneviewrs786205058
scholarrs786205058
googlers786205058
pharmgkbrs786205058
gwascentralrs786205058
openSNPrs786205058
23andMers786205058
23andMe allrs786205058
SNP Nexus

SNPshotrs786205058
SNPdbers786205058
MSV3drs786205058
GWAS Ctlgrs786205058
Max Magnitude0
ClinVar
Risk rs786205058(A;A)
Alt rs786205058(A;A)
Reference rs786205058(G;G)
Significance Pathogenic
Disease Microcytic anemia
Variation info
Gene TMPRSS6
CLNDBN Microcytic anemia
Reversed 1
HGVS NC_000022.10:g.37469571C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001466.4,