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rs10276619

From SNPedia

Orientationplus
Stabilizedplus
Make rs10276619(A;A)
Make rs10276619(A;G)
Make rs10276619(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position50273756
is asnp
is mentioned by
dbSNPrs10276619
ebirs10276619
HLIrs10276619
Exacrs10276619
Varsomers10276619
Maprs10276619
PheGenIrs10276619
hapmaprs10276619
1000 genomesrs10276619
hgdprs10276619
ensemblrs10276619
gopubmedrs10276619
geneviewrs10276619
scholarrs10276619
googlers10276619
pharmgkbrs10276619
gwascentralrs10276619
openSNPrs10276619
23andMers10276619
23andMe allrs10276619
SNP Nexus

SNPshotrs10276619
SNPdbers10276619
MSV3drs10276619
GWAS Ctlgrs10276619
GMAF0.4541
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19668339OA-icon.png]
Trait Hippocampal atrophy
Title Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease
Risk Allele
P-val 0.000003
Odds Ratio NR NR


GET Evidence
rs10276619
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.609375
summary



GWAS snp
PMID [PMID 23273568OA-icon.png]
Trait Systemic lupus erythematosus
Title Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians.
Risk Allele G
P-val 6E-6
Odds Ratio 1.18