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rs3219090

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;G) 0 common in complete genomics
Make rs3219090(A;A)
Make rs3219090(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position226376990
GenePARP1
is asnp
is mentioned by
dbSNPrs3219090
ebirs3219090
HLIrs3219090
Exacrs3219090
Varsomers3219090
Maprs3219090
PheGenIrs3219090
hapmaprs3219090
1000 genomesrs3219090
hgdprs3219090
ensemblrs3219090
gopubmedrs3219090
geneviewrs3219090
scholarrs3219090
googlers3219090
pharmgkbrs3219090
gwascentralrs3219090
openSNPrs3219090
23andMers3219090
23andMe allrs3219090
SNP Nexus

SNPshotrs3219090
SNPdbers3219090
MSV3drs3219090
GWAS Ctlgrs3219090
GMAF0.4637
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21983785OA-icon.png]
Trait
Title Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3.
Risk Allele C
P-val 9E-8
Odds Ratio 1.1500 [NR]


[PMID 23537197OA-icon.png] Genetic variants in PARP1 (rs3219090) and IRF4 (rs12203592) genes associated with melanoma susceptibility in a Spanish population


[PMID 27644669] Association of Poly (ADP-Ribose) Polymerase 1 Variants with Oral Squamous Cell Carcinoma Susceptibility in a South Indian Population.