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rs28933688

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in clinvar
Make rs28933688(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position106036662
GeneSERPINA7
is asnp
is mentioned by
dbSNPrs28933688
ebirs28933688
HLIrs28933688
Exacrs28933688
Varsomers28933688
Maprs28933688
PheGenIrs28933688
hapmaprs28933688
1000 genomesrs28933688
hgdprs28933688
ensemblrs28933688
gopubmedrs28933688
geneviewrs28933688
scholarrs28933688
googlers28933688
pharmgkbrs28933688
gwascentralrs28933688
openSNPrs28933688
23andMers28933688
23andMe allrs28933688
SNP Nexus

SNPshotrs28933688
SNPdbers28933688
MSV3drs28933688
GWAS Ctlgrs28933688
Max Magnitude0
OMIM314200
DescTHYROXINE-BINDING GLOBULIN DEFICIENCY, PARTIAL, MONTREAL TYPE
Variant0006
Relatedalso
Neighborrs2234036
Distance1285
Neighborrs28933689
Distance50


ClinVar
Risk rs28933688(C;C)
Alt rs28933688(C;C)
Reference rs28933688(G;G)
Significance Pathogenic
Disease Thyroxine-binding globulin deficiency
Variation info
Gene SERPINA7
CLNDBN Thyroxine-binding globulin deficiency, partial
Reversed 1
HGVS NC_000023.10:g.105280653C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010449.5,