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rs786205060

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205060(-;-)
Make rs786205060(-;CCCC)
Make rs786205060(CCCC;CCCC)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position37069154
GeneTMPRSS6
is asnp
is mentioned by
dbSNPrs786205060
ebirs786205060
HLIrs786205060
Exacrs786205060
Varsomers786205060
Maprs786205060
PheGenIrs786205060
hapmaprs786205060
1000 genomesrs786205060
hgdprs786205060
ensemblrs786205060
gopubmedrs786205060
geneviewrs786205060
scholarrs786205060
googlers786205060
pharmgkbrs786205060
gwascentralrs786205060
openSNPrs786205060
23andMers786205060
23andMe allrs786205060
SNP Nexus

SNPshotrs786205060
SNPdbers786205060
MSV3drs786205060
GWAS Ctlgrs786205060
Max Magnitude0
ClinVar
Risk rs786205060(CCCC;CCCC)
Alt rs786205060(CCCC;CCCC)
Reference rs786205060(;)
Significance Pathogenic
Disease Microcytic anemia
Variation info
Gene TMPRSS6
CLNDBN Microcytic anemia
Reversed 1
HGVS NC_000022.10:g.37465195_37465198dupGGGG
CLNSRC OMIM Allelic Variant
CLNACC RCV000001474.4,