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rs1511412

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs1511412(A;A)
Make rs1511412(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position138994862
is asnp
is mentioned by
dbSNPrs1511412
dbSNP (classic)rs1511412
ClinGenrs1511412
ebirs1511412
HLIrs1511412
Exacrs1511412
Gnomadrs1511412
Varsomers1511412
LitVarrs1511412
Maprs1511412
PheGenIrs1511412
Biobankrs1511412
1000 genomesrs1511412
hgdprs1511412
ensemblrs1511412
geneviewrs1511412
scholarrs1511412
googlers1511412
pharmgkbrs1511412
gwascentralrs1511412
openSNPrs1511412
23andMers1511412
SNPshotrs1511412
SNPdbers1511412
MSV3drs1511412
GWAS Ctlgrs1511412
GMAF0.06336
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 A
P-val 2E-13
Odds Ratio 1.87 [1.58-2.21]
OMIM148100
Desc
Variant
Relatedalso


[PMID 25932232OA-icon.png] SNP rs1511412 in FOXL2 gene as a risk factor for keloid by meta analysis


[PMID 29511450OA-icon.png] Genomic risk variants at 3q22.3 are associated with keloids in a Chinese Han population.