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rs587776722

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776722(C;T)
Make rs587776722(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position106034230
GeneSERPINA7
is asnp
is mentioned by
dbSNPrs587776722
ebirs587776722
HLIrs587776722
Exacrs587776722
Varsomers587776722
Maprs587776722
PheGenIrs587776722
hapmaprs587776722
1000 genomesrs587776722
hgdprs587776722
ensemblrs587776722
gopubmedrs587776722
geneviewrs587776722
scholarrs587776722
googlers587776722
pharmgkbrs587776722
gwascentralrs587776722
openSNPrs587776722
23andMers587776722
23andMe allrs587776722
SNP Nexus

SNPshotrs587776722
SNPdbers587776722
MSV3drs587776722
GWAS Ctlgrs587776722
Max Magnitude0
ClinVar
Risk rs587776722(C,T;C,T)
Alt rs587776722(C,T;C,T)
Reference rs587776722(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.105278221C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010474.5,