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rs112587690

From SNPedia

Orientationminus
Stabilizedminus
Make rs112587690(-;-)
Make rs112587690(-;GGGCCT)
Make rs112587690(GGGCCT;GGGCCT)
ReferenceGRCh37.p5 37.3/135
Chromosome11
Position534407
GeneHRAS
is asnp
is mentioned by
dbSNPrs112587690
ClinGenrs112587690
ebirs112587690
HLIrs112587690
Exacrs112587690
Varsomers112587690
Maprs112587690
PheGenIrs112587690
hapmaprs112587690
1000 genomesrs112587690
hgdprs112587690
ensemblrs112587690
gopubmedrs112587690
geneviewrs112587690
scholarrs112587690
googlers112587690
pharmgkbrs112587690
gwascentralrs112587690
openSNPrs112587690
23andMers112587690
23andMe allrs112587690
SNP Nexus

SNPshotrs112587690
SNPdbers112587690
MSV3drs112587690
GWAS Ctlgrs112587690
StatusDeleted
Max Magnitude

[PMID 22618666OA-icon.png] Association between HRAS rs12628 and rs112587690 polymorphisms with the risk of melanoma in the North American population