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rs772490052

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs772490052(C;T)
Make rs772490052(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position81143581
GeneLOC101928462, TSHR
is asnp
is mentioned by
dbSNPrs772490052
dbSNP (classic)rs772490052
ClinGenrs772490052
ebirs772490052
HLIrs772490052
Exacrs772490052
Gnomadrs772490052
Varsomers772490052
LitVarrs772490052
Maprs772490052
PheGenIrs772490052
Biobankrs772490052
1000 genomesrs772490052
hgdprs772490052
ensemblrs772490052
geneviewrs772490052
scholarrs772490052
googlers772490052
pharmgkbrs772490052
gwascentralrs772490052
openSNPrs772490052
23andMers772490052
23andMe allrs772490052
SNPshotrs772490052
SNPdbers772490052
MSV3drs772490052
GWAS Ctlgrs772490052
Max Magnitude0
ClinVar
Risk rs772490052(T;T)
Alt rs772490052(T;T)
Reference Rs772490052(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC101928431 TSHR
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.81609925C>T
CLNSRC
CLNACC RCV000487167.1,