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rs483352903

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs483352903(-;-)
Make rs483352903(-;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position106036504
GeneSERPINA7
is asnp
is mentioned by
dbSNPrs483352903
ebirs483352903
HLIrs483352903
Exacrs483352903
Varsomers483352903
Maprs483352903
PheGenIrs483352903
hapmaprs483352903
1000 genomesrs483352903
hgdprs483352903
ensemblrs483352903
gopubmedrs483352903
geneviewrs483352903
scholarrs483352903
googlers483352903
pharmgkbrs483352903
gwascentralrs483352903
openSNPrs483352903
23andMers483352903
23andMe allrs483352903
SNP Nexus

SNPshotrs483352903
SNPdbers483352903
MSV3drs483352903
GWAS Ctlgrs483352903
Max Magnitude0
ClinVar
Risk rs483352903(;)
Alt rs483352903(;)
Reference rs483352903(T;T)
Significance Pathogenic
Disease Thyroxine-binding globulin deficiency
Variation info
Gene SERPINA7
CLNDBN Thyroxine-binding globulin deficiency, complete
Reversed 1
HGVS NC_000023.10:g.105280495delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000010452.3,