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rs144120198

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs144120198(A;A)
Make rs144120198(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32443193
GeneHLA-DRA
is asnp
is mentioned by
dbSNPrs144120198
ebirs144120198
HLIrs144120198
Exacrs144120198
Varsomers144120198
Maprs144120198
PheGenIrs144120198
hapmaprs144120198
1000 genomesrs144120198
hgdprs144120198
ensemblrs144120198
gopubmedrs144120198
geneviewrs144120198
scholarrs144120198
googlers144120198
pharmgkbrs144120198
gwascentralrs144120198
openSNPrs144120198
23andMers144120198
23andMe allrs144120198
SNP Nexus

SNPshotrs144120198
SNPdbers144120198
MSV3drs144120198
GWAS Ctlgrs144120198
Max Magnitude0
ClinVar
Risk rs144120198(A;A)
Alt rs144120198(A;A)
Reference rs144120198(G;G)
Significance Untested
Disease Malignant melanoma
Variation info
Gene HLA-DRA
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000006.12:g.32443193G>A
CLNSRC ClinVar
CLNACC RCV000061399.2,


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