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rs7905537

From SNPedia

Orientationplus
Stabilizedplus
Make rs7905537(A;A)
Make rs7905537(A;C)
Make rs7905537(C;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position33942347
is asnp
is mentioned by
dbSNPrs7905537
ebirs7905537
HLIrs7905537
Exacrs7905537
Varsomers7905537
Maprs7905537
PheGenIrs7905537
hapmaprs7905537
1000 genomesrs7905537
hgdprs7905537
ensemblrs7905537
gopubmedrs7905537
geneviewrs7905537
scholarrs7905537
googlers7905537
pharmgkbrs7905537
gwascentralrs7905537
openSNPrs7905537
23andMers7905537
23andMe allrs7905537
SNP Nexus

SNPshotrs7905537
SNPdbers7905537
MSV3drs7905537
GWAS Ctlgrs7905537
GMAF0.2461
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20709820OA-icon.png]
Trait
Title Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema
Risk Allele A
P-val 8E-7
Odds Ratio 1.85 [NR] HU increase