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rs141132227

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141132227(C;T)
Make rs141132227(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32814359
GeneHLA-DOB
is asnp
is mentioned by
dbSNPrs141132227
ebirs141132227
HLIrs141132227
Exacrs141132227
Varsomers141132227
Maprs141132227
PheGenIrs141132227
hapmaprs141132227
1000 genomesrs141132227
hgdprs141132227
ensemblrs141132227
gopubmedrs141132227
geneviewrs141132227
scholarrs141132227
googlers141132227
pharmgkbrs141132227
gwascentralrs141132227
openSNPrs141132227
23andMers141132227
23andMe allrs141132227
SNP Nexus

SNPshotrs141132227
SNPdbers141132227
MSV3drs141132227
GWAS Ctlgrs141132227
Max Magnitude0
ClinVar
Risk rs141132227(T;T)
Alt rs141132227(T;T)
Reference rs141132227(C;C)
Significance Untested
Disease Malignant melanoma
Variation info
Gene HLA-DOB
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000006.12:g.32814359C>T
CLNSRC ClinVar
CLNACC RCV000061401.2,


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