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rs121918676

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918676(A;A)
Make rs121918676(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position133756969
GeneTF
is asnp
is mentioned by
dbSNPrs121918676
ebirs121918676
HLIrs121918676
Exacrs121918676
Varsomers121918676
Maprs121918676
PheGenIrs121918676
hapmaprs121918676
1000 genomesrs121918676
hgdprs121918676
ensemblrs121918676
gopubmedrs121918676
geneviewrs121918676
scholarrs121918676
googlers121918676
pharmgkbrs121918676
gwascentralrs121918676
openSNPrs121918676
23andMers121918676
23andMe allrs121918676
SNP Nexus

SNPshotrs121918676
SNPdbers121918676
MSV3drs121918676
GWAS Ctlgrs121918676
Max Magnitude0
OMIM190000
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918676(A;A)
Alt rs121918676(A;A)
Reference rs121918676(G;G)
Significance Pathogenic
Disease Transferrin variant d1
Variation info
Gene TF
CLNDBN Transferrin variant d1
Reversed 0
HGVS NC_000003.11:g.133475813G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013448.24,