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rs144045930

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs144045930(C;T)
Make rs144045930(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position33068660
GeneHLA-DPA1
is asnp
is mentioned by
dbSNPrs144045930
ebirs144045930
HLIrs144045930
Exacrs144045930
Varsomers144045930
Maprs144045930
PheGenIrs144045930
hapmaprs144045930
1000 genomesrs144045930
hgdprs144045930
ensemblrs144045930
gopubmedrs144045930
geneviewrs144045930
scholarrs144045930
googlers144045930
pharmgkbrs144045930
gwascentralrs144045930
openSNPrs144045930
23andMers144045930
23andMe allrs144045930
SNP Nexus

SNPshotrs144045930
SNPdbers144045930
MSV3drs144045930
GWAS Ctlgrs144045930
Max Magnitude0
ClinVar
Risk rs144045930(T;T)
Alt rs144045930(T;T)
Reference rs144045930(C;C)
Significance Untested
Disease Malignant melanoma
Variation info
Gene HLA-DPA1
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000006.12:g.33068660C>T
CLNSRC ClinVar
CLNACC RCV000061404.2,


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