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rs121918678

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918678(A;G)
Make rs121918678(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position133777112
GeneTF
is asnp
is mentioned by
dbSNPrs121918678
ebirs121918678
HLIrs121918678
Exacrs121918678
Varsomers121918678
Maprs121918678
PheGenIrs121918678
hapmaprs121918678
1000 genomesrs121918678
hgdprs121918678
ensemblrs121918678
gopubmedrs121918678
geneviewrs121918678
scholarrs121918678
googlers121918678
pharmgkbrs121918678
gwascentralrs121918678
openSNPrs121918678
23andMers121918678
23andMe allrs121918678
SNP Nexus

SNPshotrs121918678
SNPdbers121918678
MSV3drs121918678
GWAS Ctlgrs121918678
Max Magnitude0
OMIM190000
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121918678(G;G)
Alt rs121918678(G;G)
Reference rs121918678(A;A)
Significance Pathogenic
Disease Transferrin variant bv
Variation info
Gene TF
CLNDBN Transferrin variant bv
Reversed 0
HGVS NC_000003.11:g.133495956A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000013453.16,