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rs587776719

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776719(-;-)
Make rs587776719(-;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position106033634
GeneSERPINA7
is asnp
is mentioned by
dbSNPrs587776719
ebirs587776719
HLIrs587776719
Exacrs587776719
Varsomers587776719
Maprs587776719
PheGenIrs587776719
hapmaprs587776719
1000 genomesrs587776719
hgdprs587776719
ensemblrs587776719
gopubmedrs587776719
geneviewrs587776719
scholarrs587776719
googlers587776719
pharmgkbrs587776719
gwascentralrs587776719
openSNPrs587776719
23andMers587776719
23andMe allrs587776719
SNP Nexus

SNPshotrs587776719
SNPdbers587776719
MSV3drs587776719
GWAS Ctlgrs587776719
Max Magnitude0
ClinVar
Risk rs587776719(;)
Alt rs587776719(;)
Reference rs587776719(G;G)
Significance Pathogenic
Disease Thyroxine-binding globulin deficiency
Variation info
Gene SERPINA7
CLNDBN Thyroxine-binding globulin deficiency, complete
Reversed 0
HGVS NC_000023.10:g.105277625delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000010457.3,