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rs1057519028

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519028(G;G)
Make rs1057519028(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position24122919
GeneTHRB
is asnp
is mentioned by
dbSNPrs1057519028
dbSNP (old)rs1057519028
ClinGenrs1057519028
ebirs1057519028
HLIrs1057519028
Exacrs1057519028
Gnomadrs1057519028
Varsomers1057519028
Maprs1057519028
PheGenIrs1057519028
Biobankrs1057519028
1000 genomesrs1057519028
hgdprs1057519028
ensemblrs1057519028
gopubmedrs1057519028
geneviewrs1057519028
scholarrs1057519028
googlers1057519028
pharmgkbrs1057519028
gwascentralrs1057519028
openSNPrs1057519028
23andMers1057519028
23andMe allrs1057519028
SNPshotrs1057519028
SNPdbers1057519028
MSV3drs1057519028
GWAS Ctlgrs1057519028
Max Magnitude0
ClinVar
Risk rs1057519028(G;G)
Alt rs1057519028(G;G)
Reference Rs1057519028(T;T)
Significance Probable-Pathogenic
Disease Thyroid hormone resistance
Variation info
Gene THRB
CLNDBN Thyroid hormone resistance, generalized, autosomal dominant
Reversed 1
HGVS NC_000003.11:g.24164410A>C
CLNSRC
CLNACC RCV000416319.1,