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rs1060499695

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499695(A;G)
Make rs1060499695(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position24127666
GeneTHRB
is asnp
is mentioned by
dbSNPrs1060499695
dbSNP (old)rs1060499695
ClinGenrs1060499695
ebirs1060499695
HLIrs1060499695
Exacrs1060499695
Gnomadrs1060499695
Varsomers1060499695
Maprs1060499695
PheGenIrs1060499695
Biobankrs1060499695
1000 genomesrs1060499695
hgdprs1060499695
ensemblrs1060499695
gopubmedrs1060499695
geneviewrs1060499695
scholarrs1060499695
googlers1060499695
pharmgkbrs1060499695
gwascentralrs1060499695
openSNPrs1060499695
23andMers1060499695
23andMe allrs1060499695
SNPshotrs1060499695
SNPdbers1060499695
MSV3drs1060499695
GWAS Ctlgrs1060499695
Max Magnitude0
ClinVar
Risk rs1060499695(G;G)
Alt rs1060499695(G;G)
Reference Rs1060499695(A;A)
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.24169157T>C
CLNSRC
CLNACC RCV000449629.1,