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rs10774625

From SNPedia

Orientationplus
Stabilizedplus
Make rs10774625(A;A)
Make rs10774625(A;G)
Make rs10774625(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position111472415
GeneATXN2
is asnp
is mentioned by
dbSNPrs10774625
ebirs10774625
HLIrs10774625
Exacrs10774625
Varsomers10774625
Maprs10774625
PheGenIrs10774625
hapmaprs10774625
1000 genomesrs10774625
hgdprs10774625
ensemblrs10774625
gopubmedrs10774625
geneviewrs10774625
scholarrs10774625
googlers10774625
pharmgkbrs10774625
gwascentralrs10774625
openSNPrs10774625
23andMers10774625
23andMe allrs10774625
SNP Nexus

SNPshotrs10774625
SNPdbers10774625
MSV3drs10774625
GWAS Ctlgrs10774625
GMAF0.225
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21060863OA-icon.png]
Trait
Title Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo
Risk Allele A
P-val 2E-13
Odds Ratio 1.5000 [1.11-1.89] um increase


[PMID 23844121OA-icon.png] Thrombotic Antiphospholipid Syndrome Shows Strong Haplotypic Association with SH2B3-ATXN2 Locus