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rs1085307573

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome14
Position81091094
GeneLOC101928462, TSHR
is asnp
is mentioned by
dbSNPrs1085307573
dbSNP (old)rs1085307573
ClinGenrs1085307573
ebirs1085307573
HLIrs1085307573
Exacrs1085307573
Gnomadrs1085307573
Varsomers1085307573
LitVarrs1085307573
Maprs1085307573
PheGenIrs1085307573
Biobankrs1085307573
1000 genomesrs1085307573
hgdprs1085307573
ensemblrs1085307573
gopubmedrs1085307573
geneviewrs1085307573
scholarrs1085307573
googlers1085307573
pharmgkbrs1085307573
gwascentralrs1085307573
openSNPrs1085307573
23andMers1085307573
23andMe allrs1085307573
SNPshotrs1085307573
SNPdbers1085307573
MSV3drs1085307573
GWAS Ctlgrs1085307573
Max Magnitude0
ClinVar
Risk rs1085307573(-;-)
Alt rs1085307573(-;-)
Reference Rs1085307573(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC101928462 TSHR
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.81557438delA
CLNSRC
CLNACC RCV000489917.1,