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rs9945924

From SNPedia

Orientationplus
Stabilizedplus
Make rs9945924(A;A)
Make rs9945924(A;G)
Make rs9945924(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position63953532
GeneHMSD
is asnp
is mentioned by
dbSNPrs9945924
ebirs9945924
HLIrs9945924
Exacrs9945924
Varsomers9945924
Maprs9945924
PheGenIrs9945924
hapmaprs9945924
1000 genomesrs9945924
hgdprs9945924
ensemblrs9945924
gopubmedrs9945924
geneviewrs9945924
scholarrs9945924
googlers9945924
pharmgkbrs9945924
gwascentralrs9945924
openSNPrs9945924
23andMers9945924
23andMe allrs9945924
SNP Nexus

SNPshotrs9945924
SNPdbers9945924
MSV3drs9945924
GWAS Ctlgrs9945924
GMAF0.2663
Max Magnitude
? (A;A) (A;G) (G;G) 28
OMIM612086
DescMINOR HISTOCOMPATIBILITY ANTIGEN, SERPIN DOMAIN-CONTAINING; HMSD
Variant
Relatedalso
[PMID 19001137OA-icon.png] Toward targeting B cell cancers with CD4+ CTLs: identification of a CD19-encoded minor histocompatibility antigen using a novel genome-wide analysis.