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rs145420390

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs145420390(A;A)
Make rs145420390(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position3848618
GeneCEP104
is asnp
is mentioned by
dbSNPrs145420390
ebirs145420390
HLIrs145420390
Exacrs145420390
Varsomers145420390
Maprs145420390
PheGenIrs145420390
hapmaprs145420390
1000 genomesrs145420390
hgdprs145420390
ensemblrs145420390
gopubmedrs145420390
geneviewrs145420390
scholarrs145420390
googlers145420390
pharmgkbrs145420390
gwascentralrs145420390
openSNPrs145420390
23andMers145420390
23andMe allrs145420390
SNP Nexus

SNPshotrs145420390
SNPdbers145420390
MSV3drs145420390
GWAS Ctlgrs145420390
Max Magnitude0
ClinVar
Risk rs145420390(A;A)
Alt rs145420390(A;A)
Reference rs145420390(G;G)
Significance Untested
Disease Malignant melanoma
Variation info
Gene CEP104
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000001.11:g.3848618G>A
CLNSRC ClinVar
CLNACC RCV000060190.2,


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