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rs10162002

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs10162002(A;A)
Make rs10162002(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position23468371
GeneLINC00327
is asnp
is mentioned by
dbSNPrs10162002
ebirs10162002
HLIrs10162002
Exacrs10162002
Varsomers10162002
Maprs10162002
PheGenIrs10162002
hapmaprs10162002
1000 genomesrs10162002
hgdprs10162002
ensemblrs10162002
gopubmedrs10162002
geneviewrs10162002
scholarrs10162002
googlers10162002
pharmgkbrs10162002
gwascentralrs10162002
openSNPrs10162002
23andMers10162002
23andMe allrs10162002
SNP Nexus

SNPshotrs10162002
SNPdbers10162002
MSV3drs10162002
GWAS Ctlgrs10162002
GMAF0.1648
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22493691OA-icon.png]
Trait
Title Novel associations for hypothyroidism include known autoimmune risk loci.
Risk Allele A
P-val 0.000005
Odds Ratio 1.2330 None