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rs2284063

From SNPedia

Orientationplus
Stabilizedplus
Make rs2284063(A;A)
Make rs2284063(A;G)
Make rs2284063(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position38148291
GenePLA2G6
is asnp
is mentioned by
dbSNPrs2284063
ebirs2284063
HLIrs2284063
Exacrs2284063
Varsomers2284063
Maprs2284063
PheGenIrs2284063
hapmaprs2284063
1000 genomesrs2284063
hgdprs2284063
ensemblrs2284063
gopubmedrs2284063
geneviewrs2284063
scholarrs2284063
googlers2284063
pharmgkbrs2284063
gwascentralrs2284063
openSNPrs2284063
23andMers2284063
23andMe allrs2284063
SNP Nexus

SNPshotrs2284063
SNPdbers2284063
MSV3drs2284063
GWAS Ctlgrs2284063
GMAF0.3678
Max Magnitude
? (A;A) (A;G) (G;G) 28
23andMe blog rs2284063 A 1.20 Melanoma
GWAS snp
PMID [PMID 19578364OA-icon.png]
Trait Melanoma
Title Genome-wide association study identifies three loci associated with melanoma risk
Risk Allele
P-val 2E-9
Odds Ratio 1.20 [1.14-1.28]
GWAS snp
PMID [PMID 19578365OA-icon.png]
Trait Cutaneous nevi
Title Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi
Risk Allele G
P-val 3E-8
Odds Ratio 0.08 [-0.002-0.16] decrease in log nevus count
OMIM155601
Desc
Variant
Relatedalso
OMIM162900
Desc
Variant
Relatedalso
[PMID 19686382OA-icon.png] Genome-wide associations studies for melanoma and nevi.


[PMID 22459563] Association between PLA2G6 gene polymorphisms and Parkinson's disease in the Chinese Han population.


GET Evidence
rs2284063
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.453125
summary