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rs7148590

From SNPedia

Orientationplus
Stabilizedplus
Make rs7148590(A;A)
Make rs7148590(A;G)
Make rs7148590(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position65006478
GeneCHURC1-FNTB, FNTB, MAX
is asnp
is mentioned by
dbSNPrs7148590
ebirs7148590
HLIrs7148590
Exacrs7148590
Varsomers7148590
Maprs7148590
PheGenIrs7148590
hapmaprs7148590
1000 genomesrs7148590
hgdprs7148590
ensemblrs7148590
gopubmedrs7148590
geneviewrs7148590
scholarrs7148590
googlers7148590
pharmgkbrs7148590
gwascentralrs7148590
openSNPrs7148590
23andMers7148590
23andMe allrs7148590
SNP Nexus

SNPshotrs7148590
SNPdbers7148590
MSV3drs7148590
GWAS Ctlgrs7148590
GMAF0.4353
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23720494OA-icon.png]
Trait Blood trace element (Zn levels)
Title Genome-wide association study identifies loci affecting blood copper, selenium and zinc.
Risk Allele
P-val 1E-7
Odds Ratio .14 [0.089-0.191] unit increase