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rs139984517

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139984517(A;A)
Make rs139984517(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position3763705
GeneCCDC27
is asnp
is mentioned by
dbSNPrs139984517
ebirs139984517
HLIrs139984517
Exacrs139984517
Varsomers139984517
Maprs139984517
PheGenIrs139984517
hapmaprs139984517
1000 genomesrs139984517
hgdprs139984517
ensemblrs139984517
gopubmedrs139984517
geneviewrs139984517
scholarrs139984517
googlers139984517
pharmgkbrs139984517
gwascentralrs139984517
openSNPrs139984517
23andMers139984517
23andMe allrs139984517
SNP Nexus

SNPshotrs139984517
SNPdbers139984517
MSV3drs139984517
GWAS Ctlgrs139984517
Max Magnitude0
ClinVar
Risk rs139984517(A;A)
Alt rs139984517(A;A)
Reference rs139984517(G;G)
Significance Untested
Disease Malignant melanoma
Variation info
Gene CCDC27
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000001.11:g.3763705G>A
CLNSRC ClinVar
CLNACC RCV000060186.2,


[PMID 21499247OA-icon.png] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.