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rs7671167

From SNPedia

Orientationplus
Stabilizedplus
Make rs7671167(C;C)
Make rs7671167(C;T)
Make rs7671167(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position88962828
GeneFAM13A
is asnp
is mentioned by
dbSNPrs7671167
ebirs7671167
HLIrs7671167
Exacrs7671167
Varsomers7671167
Maprs7671167
PheGenIrs7671167
hapmaprs7671167
1000 genomesrs7671167
hgdprs7671167
ensemblrs7671167
gopubmedrs7671167
geneviewrs7671167
scholarrs7671167
googlers7671167
pharmgkbrs7671167
gwascentralrs7671167
openSNPrs7671167
23andMers7671167
23andMe allrs7671167
SNP Nexus

SNPshotrs7671167
SNPdbers7671167
MSV3drs7671167
GWAS Ctlgrs7671167
GMAF0.4858
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20173748OA-icon.png]
Trait Chronic obstructive pulmonary disease
Title Variants in FAM13A are associated with chronic obstructive pulmonary disease
Risk Allele
P-val 1E-11
Odds Ratio 1.32 [1.19-1.47]
OMIM606963
Desc
Variant
Relatedalso
[PMID 21304900OA-icon.png] Individual and cumulative effects of GWAS susceptibility loci in lung cancer: associations after sub-phenotyping for COPD.


[PMID 23891779] Association of FAM13A polymorphisms with COPD and COPD-related phenotypes in Han Chinese


[PMID 25154699OA-icon.png] Phenotypic and genetic heterogeneity among subjects with mild airflow obstruction in COPDGene


[PMID 26251585OA-icon.png] Variants in multiple genes polymorphism association analysis of COPD in the Chinese Li population