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rs1175550

From SNPedia

Orientationminus
Stabilizedplus
Make rs1175550(C;C)
Make rs1175550(C;T)
Make rs1175550(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position3774964
GeneSMIM1
is asnp
is mentioned by
dbSNPrs1175550
ebirs1175550
HLIrs1175550
Exacrs1175550
Varsomers1175550
Maprs1175550
PheGenIrs1175550
hapmaprs1175550
1000 genomesrs1175550
hgdprs1175550
ensemblrs1175550
gopubmedrs1175550
geneviewrs1175550
scholarrs1175550
googlers1175550
pharmgkbrs1175550
gwascentralrs1175550
openSNPrs1175550
23andMers1175550
23andMe allrs1175550
SNP Nexus

SNPshotrs1175550
SNPdbers1175550
MSV3drs1175550
GWAS Ctlgrs1175550
GMAF0.2346
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23720494OA-icon.png]
Trait Blood trace element (Cu levels)
Title Genome-wide association study identifies loci affecting blood copper, selenium and zinc.
Risk Allele A
P-val 5E-10
Odds Ratio .20 [0.14-0.26] unit decrease


[PMID 23563608OA-icon.png] SMIM1 underlies the Vel blood group and influences red blood cell traits.