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rs1064794318

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(GCAG;GCAG) 0 common in clinvar
Chromosome14
Position81068278
GeneLOC101928462, TSHR
is asnp
is mentioned by
dbSNPrs1064794318
dbSNP (old)rs1064794318
ClinGenrs1064794318
ebirs1064794318
HLIrs1064794318
Exacrs1064794318
Gnomadrs1064794318
Varsomers1064794318
Maprs1064794318
PheGenIrs1064794318
Biobankrs1064794318
1000 genomesrs1064794318
hgdprs1064794318
ensemblrs1064794318
gopubmedrs1064794318
geneviewrs1064794318
scholarrs1064794318
googlers1064794318
pharmgkbrs1064794318
gwascentralrs1064794318
openSNPrs1064794318
23andMers1064794318
23andMe allrs1064794318
SNPshotrs1064794318
SNPdbers1064794318
MSV3drs1064794318
GWAS Ctlgrs1064794318
Max Magnitude0
ClinVar
Risk rs1064794318(TCCT;TCCT)
Alt rs1064794318(TCCT;TCCT)
Reference Rs1064794318(GCAG;GCAG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TSHR
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.81534622_81534625delGCAGinsTCCT
CLNSRC
CLNACC RCV000483426.1,