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rs10248351

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs10248351(C;C)
Make rs10248351(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position88852128
GeneZNF804B
is asnp
is mentioned by
dbSNPrs10248351
ebirs10248351
HLIrs10248351
Exacrs10248351
Varsomers10248351
Maprs10248351
PheGenIrs10248351
hapmaprs10248351
1000 genomesrs10248351
hgdprs10248351
ensemblrs10248351
gopubmedrs10248351
geneviewrs10248351
scholarrs10248351
googlers10248351
pharmgkbrs10248351
gwascentralrs10248351
openSNPrs10248351
23andMers10248351
23andMe allrs10248351
SNP Nexus

SNPshotrs10248351
SNPdbers10248351
MSV3drs10248351
GWAS Ctlgrs10248351
GMAF0.04867
Max Magnitude0
? (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 1.8430 None