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rs1485993

From SNPedia

Orientationminus
Stabilizedminus
Make rs1485993(C;C)
Make rs1485993(C;T)
Make rs1485993(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position69547646
is asnp
is mentioned by
dbSNPrs1485993
ebirs1485993
HLIrs1485993
Exacrs1485993
Varsomers1485993
Maprs1485993
PheGenIrs1485993
hapmaprs1485993
1000 genomesrs1485993
hgdprs1485993
ensemblrs1485993
gopubmedrs1485993
geneviewrs1485993
scholarrs1485993
googlers1485993
pharmgkbrs1485993
gwascentralrs1485993
openSNPrs1485993
23andMers1485993
23andMe allrs1485993
SNP Nexus

SNPshotrs1485993
SNPdbers1485993
MSV3drs1485993
GWAS Ctlgrs1485993
GMAF0.3994
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23537197OA-icon.png] Genetic variants in PARP1 (rs3219090) and IRF4 (rs12203592) genes associated with melanoma susceptibility in a Spanish population


[PMID 21983787OA-icon.png] Genome-wide association study identifies three new melanoma susceptibility loci.