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rs139901107

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139901107(A;A)
Make rs139901107(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position3839017
GeneCEP104
is asnp
is mentioned by
dbSNPrs139901107
ebirs139901107
HLIrs139901107
Exacrs139901107
Varsomers139901107
Maprs139901107
PheGenIrs139901107
hapmaprs139901107
1000 genomesrs139901107
hgdprs139901107
ensemblrs139901107
gopubmedrs139901107
geneviewrs139901107
scholarrs139901107
googlers139901107
pharmgkbrs139901107
gwascentralrs139901107
openSNPrs139901107
23andMers139901107
23andMe allrs139901107
SNP Nexus

SNPshotrs139901107
SNPdbers139901107
MSV3drs139901107
GWAS Ctlgrs139901107
Max Magnitude0
ClinVar
Risk rs139901107(A;A)
Alt rs139901107(A;A)
Reference rs139901107(G;G)
Significance Untested
Disease Malignant melanoma
Variation info
Gene CEP104
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000001.11:g.3839017G>A
CLNSRC ClinVar
CLNACC RCV000060189.2,


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