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rs873549

From SNPedia

Orientationminus
Stabilizedminus
Make rs873549(A;A)
Make rs873549(A;G)
Make rs873549(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position222098425
is asnp
is mentioned by
dbSNPrs873549
dbSNP (classic)rs873549
ClinGenrs873549
ebirs873549
HLIrs873549
Exacrs873549
Gnomadrs873549
Varsomers873549
LitVarrs873549
Maprs873549
PheGenIrs873549
Biobankrs873549
1000 genomesrs873549
hgdprs873549
ensemblrs873549
geneviewrs873549
scholarrs873549
googlers873549
pharmgkbrs873549
gwascentralrs873549
openSNPrs873549
23andMers873549
SNPshotrs873549
SNPdbers873549
MSV3drs873549
GWAS Ctlgrs873549
GMAF0.292
Max Magnitude0
? (A;A) (A;G) (G;G) 28


23andMe blog

rs873549 C 1.77x risk of keloids

rs1511412 A 1.87x

rs8032158 C 1.51x

GWAS snp
PMID [PMID 20711176]
Trait
Title A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population
Risk Allele C
P-val 6E-23
Odds Ratio 1.77 [1.58-1.99]
OMIM148100
Desc
Variant
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