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

rs587776721

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(TG;TG) 0 common in clinvar
Make rs587776721(-;-)
Make rs587776721(-;A)
ReferenceGRCh38 38.1/142
ChromosomeX
Position106036885
GeneSERPINA7
is asnp
is mentioned by
dbSNPrs587776721
ebirs587776721
HLIrs587776721
Exacrs587776721
Varsomers587776721
Maprs587776721
PheGenIrs587776721
hapmaprs587776721
1000 genomesrs587776721
hgdprs587776721
ensemblrs587776721
gopubmedrs587776721
geneviewrs587776721
scholarrs587776721
googlers587776721
pharmgkbrs587776721
gwascentralrs587776721
openSNPrs587776721
23andMers587776721
23andMe allrs587776721
SNP Nexus

SNPshotrs587776721
SNPdbers587776721
MSV3drs587776721
GWAS Ctlgrs587776721
Max Magnitude0
ClinVar
Risk rs587776721(AG,G;AG,G)
Alt rs587776721(AG,G;AG,G)
Reference rs587776721(TG;TG)
Significance Pathogenic
Disease Thyroxine-binding globulin deficiency
Variation info
Gene SERPINA7
CLNDBN Thyroxine-binding globulin deficiency, complete
Reversed 1
HGVS NC_000023.10:g.105280876delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000010469.3,