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rs144003672

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs144003672(A;A)
Make rs144003672(A;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position1309724
GenePUSL1
is asnp
is mentioned by
dbSNPrs144003672
ebirs144003672
HLIrs144003672
Exacrs144003672
Varsomers144003672
Maprs144003672
PheGenIrs144003672
hapmaprs144003672
1000 genomesrs144003672
hgdprs144003672
ensemblrs144003672
gopubmedrs144003672
geneviewrs144003672
scholarrs144003672
googlers144003672
pharmgkbrs144003672
gwascentralrs144003672
openSNPrs144003672
23andMers144003672
23andMe allrs144003672
SNP Nexus

SNPshotrs144003672
SNPdbers144003672
MSV3drs144003672
GWAS Ctlgrs144003672
Max Magnitude0
[PMID 21499247OA-icon.png] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
ClinVar
Risk rs144003672(A;A)
Alt rs144003672(A;A)
Reference rs144003672(C;C)
Significance Untested
Disease Malignant melanoma
Variation info
Gene ACAP3 PUSL1
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000001.11:g.1309724C>A
CLNSRC ClinVar
CLNACC RCV000059856.2,