Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909496

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909496(A;A)
Make rs121909496(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position106034380
GeneSERPINA7
is asnp
is mentioned by
dbSNPrs121909496
ebirs121909496
HLIrs121909496
Exacrs121909496
Varsomers121909496
Maprs121909496
PheGenIrs121909496
hapmaprs121909496
1000 genomesrs121909496
hgdprs121909496
ensemblrs121909496
gopubmedrs121909496
geneviewrs121909496
scholarrs121909496
googlers121909496
pharmgkbrs121909496
gwascentralrs121909496
openSNPrs121909496
23andMers121909496
23andMe allrs121909496
SNP Nexus

SNPshotrs121909496
SNPdbers121909496
MSV3drs121909496
GWAS Ctlgrs121909496
Max Magnitude0
OMIM314200
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121909496(A;A)
Alt rs121909496(A;A)
Reference rs121909496(G;G)
Significance Pathogenic
Disease Thyroxine-binding globulin deficiency
Variation info
Gene SERPINA7
CLNDBN Thyroxine-binding globulin deficiency, complete
Reversed 1
HGVS NC_000023.10:g.105278371C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010464.4,