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rs786204790

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs786204790(-;-)
Make rs786204790(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position81092610
GeneLOC101928462, TSHR
is asnp
is mentioned by
dbSNPrs786204790
ebirs786204790
HLIrs786204790
Exacrs786204790
Varsomers786204790
Maprs786204790
PheGenIrs786204790
hapmaprs786204790
1000 genomesrs786204790
hgdprs786204790
ensemblrs786204790
gopubmedrs786204790
geneviewrs786204790
scholarrs786204790
googlers786204790
pharmgkbrs786204790
gwascentralrs786204790
openSNPrs786204790
23andMers786204790
23andMe allrs786204790
SNP Nexus

SNPshotrs786204790
SNPdbers786204790
MSV3drs786204790
GWAS Ctlgrs786204790
Max Magnitude0
ClinVar
Risk rs786204790(;)
Alt rs786204790(;)
Reference rs786204790(TG;TG)
Significance Probable-Pathogenic
Disease Hypothyroidism
Variation info
Gene LOC101928462 TSHR
CLNDBN Hypothyroidism, congenital, nongoitrous, 1
Reversed 0
HGVS NC_000014.8:g.81558954_81558955delTG
CLNSRC
CLNACC RCV000169681.1,