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rs947474

From SNPedia

Orientationplus
Stabilizedplus
Make rs947474(A;A)
Make rs947474(A;G)
Make rs947474(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position6348488
GeneFCGR2C
is asnp
is mentioned by
dbSNPrs947474
ebirs947474
HLIrs947474
Exacrs947474
Varsomers947474
Maprs947474
PheGenIrs947474
hapmaprs947474
1000 genomesrs947474
hgdprs947474
ensemblrs947474
gopubmedrs947474
geneviewrs947474
scholarrs947474
googlers947474
pharmgkbrs947474
gwascentralrs947474
openSNPrs947474
23andMers947474
23andMe allrs947474
SNP Nexus

SNPshotrs947474
SNPdbers947474
MSV3drs947474
GWAS Ctlgrs947474
GMAF0.1997
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18978792OA-icon.png]
Trait Type 1 diabetes
Title Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci
Risk Allele G
P-val 4.0000000000000002E-9
Odds Ratio 1.10 [1.03-1.18]
OMIM222100
DescDIABETES MELLITUS, INSULIN-DEPENDENT; IDDM
Variant
Relatedalso
[PMID 20736230OA-icon.png] A ChIP-seq defined genome-wide map of vitamin D receptor binding: Associations with disease and evolution



[PMID 19073967OA-icon.png] Shared and distinct genetic variants in type 1 diabetes and celiac disease.


GET Evidence
rs947474
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.773438
summary



GWAS snp
PMID [PMID 24390342OA-icon.png]
Trait Rheumatoid arthritis
Title Genetics of rheumatoid arthritis contributes to biology and drug discovery.
Risk Allele A
P-val 3E-10
Odds Ratio 1.12 [1.08-1.16]