Have questions? Visit https://www.reddit.com/r/SNPedia

rs144480582

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs144480582(A;A)
Make rs144480582(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position15768540
GeneFBLIM1
is asnp
is mentioned by
dbSNPrs144480582
ebirs144480582
HLIrs144480582
Exacrs144480582
Varsomers144480582
Maprs144480582
PheGenIrs144480582
hapmaprs144480582
1000 genomesrs144480582
hgdprs144480582
ensemblrs144480582
gopubmedrs144480582
geneviewrs144480582
scholarrs144480582
googlers144480582
pharmgkbrs144480582
gwascentralrs144480582
openSNPrs144480582
23andMers144480582
23andMe allrs144480582
SNP Nexus

SNPshotrs144480582
SNPdbers144480582
MSV3drs144480582
GWAS Ctlgrs144480582
Max Magnitude0

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

ClinVar
Risk rs144480582(A;A)
Alt rs144480582(A;A)
Reference rs144480582(G;G)
Significance Untested
Disease Malignant melanoma
Variation info
Gene FBLIM1
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000001.11:g.15768540G>A
CLNSRC ClinVar
CLNACC RCV000059967.2,