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rs148699775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs148699775(A;A)
Make rs148699775(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32581815
GeneHLA-DRB1
is asnp
is mentioned by
dbSNPrs148699775
ebirs148699775
HLIrs148699775
Exacrs148699775
Varsomers148699775
Maprs148699775
PheGenIrs148699775
hapmaprs148699775
1000 genomesrs148699775
hgdprs148699775
ensemblrs148699775
gopubmedrs148699775
geneviewrs148699775
scholarrs148699775
googlers148699775
pharmgkbrs148699775
gwascentralrs148699775
openSNPrs148699775
23andMers148699775
23andMe allrs148699775
SNP Nexus

SNPshotrs148699775
SNPdbers148699775
MSV3drs148699775
GWAS Ctlgrs148699775
Max Magnitude0
ClinVar
Risk rs148699775(A;A)
Alt rs148699775(A;A)
Reference rs148699775(G;G)
Significance Untested
Disease Malignant melanoma
Variation info
Gene LOC105369230 HLA-DRB1
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000006.12:g.32581815G>A
CLNSRC ClinVar
CLNACC RCV000061400.2,


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