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rs10519980

From SNPedia

Orientationplus
Stabilizedplus
Make rs10519980(C;C)
Make rs10519980(C;T)
Make rs10519980(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position148713873
is asnp
is mentioned by
dbSNPrs10519980
ebirs10519980
HLIrs10519980
Exacrs10519980
Varsomers10519980
Maprs10519980
PheGenIrs10519980
hapmaprs10519980
1000 genomesrs10519980
hgdprs10519980
ensemblrs10519980
gopubmedrs10519980
geneviewrs10519980
scholarrs10519980
googlers10519980
pharmgkbrs10519980
gwascentralrs10519980
openSNPrs10519980
23andMers10519980
23andMe allrs10519980
SNP Nexus

SNPshotrs10519980
SNPdbers10519980
MSV3drs10519980
GWAS Ctlgrs10519980
GMAF0.1708
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22493691OA-icon.png]
Trait
Title Novel associations for hypothyroidism include known autoimmune risk loci.
Risk Allele C
P-val 0.000007
Odds Ratio 1.1600 None