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

rs61754490

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs61754490(A;T)
Make rs61754490(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position106034293
GeneSERPINA7
is asnp
is mentioned by
dbSNPrs61754490
ebirs61754490
HLIrs61754490
Exacrs61754490
Varsomers61754490
Maprs61754490
PheGenIrs61754490
hapmaprs61754490
1000 genomesrs61754490
hgdprs61754490
ensemblrs61754490
gopubmedrs61754490
geneviewrs61754490
scholarrs61754490
googlers61754490
pharmgkbrs61754490
gwascentralrs61754490
openSNPrs61754490
23andMers61754490
23andMe allrs61754490
SNP Nexus

SNPshotrs61754490
SNPdbers61754490
MSV3drs61754490
GWAS Ctlgrs61754490
GMAF0.0
Max Magnitude0
OMIM314200
Desc
Variant0010
Relatedalso
ClinVar
Risk rs61754490(T;T)
Alt rs61754490(T;T)
Reference rs61754490(A;A)
Significance Pathogenic
Disease Thyroxine-binding globulin
Variation info
Gene SERPINA7
CLNDBN Thyroxine-binding globulin, Chicago
Reversed 1
HGVS NC_000023.10:g.105278284T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010459.6,