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rs587776720

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776720(C;C)
Make rs587776720(C;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position106035387
GeneSERPINA7
is asnp
is mentioned by
dbSNPrs587776720
ebirs587776720
HLIrs587776720
Exacrs587776720
Varsomers587776720
Maprs587776720
PheGenIrs587776720
hapmaprs587776720
1000 genomesrs587776720
hgdprs587776720
ensemblrs587776720
gopubmedrs587776720
geneviewrs587776720
scholarrs587776720
googlers587776720
pharmgkbrs587776720
gwascentralrs587776720
openSNPrs587776720
23andMers587776720
23andMe allrs587776720
SNP Nexus

SNPshotrs587776720
SNPdbers587776720
MSV3drs587776720
GWAS Ctlgrs587776720
Max Magnitude0
ClinVar
Risk rs587776720(C;C)
Alt rs587776720(C;C)
Reference rs587776720(T;T)
Significance Pathogenic
Disease Thyroxine-binding globulin deficiency
Variation info
Gene SERPINA7
CLNDBN Thyroxine-binding globulin deficiency, complete
Reversed 0
HGVS NC_000023.10:g.105279378T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010467.3,