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rs786205080

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205080(C;C)
Make rs786205080(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position81092611
GeneLOC101928462, TSHR
is asnp
is mentioned by
dbSNPrs786205080
ebirs786205080
HLIrs786205080
Exacrs786205080
Varsomers786205080
Maprs786205080
PheGenIrs786205080
hapmaprs786205080
1000 genomesrs786205080
hgdprs786205080
ensemblrs786205080
gopubmedrs786205080
geneviewrs786205080
scholarrs786205080
googlers786205080
pharmgkbrs786205080
gwascentralrs786205080
openSNPrs786205080
23andMers786205080
23andMe allrs786205080
SNP Nexus

SNPshotrs786205080
SNPdbers786205080
MSV3drs786205080
GWAS Ctlgrs786205080
Max Magnitude0
ClinVar
Risk rs786205080(C;C)
Alt rs786205080(C;C)
Reference rs786205080(G;G)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene LOC101928462 TSHR
CLNDBN Hypothyroidism, congenital, nongoitrous, 1
Reversed 0
HGVS NC_000014.8:g.81558955G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006832.4,