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rs41553319

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41553319(A;A)
Make rs41553319(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943350
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41553319
ebirs41553319
HLIrs41553319
Exacrs41553319
Varsomers41553319
Maprs41553319
PheGenIrs41553319
hapmaprs41553319
1000 genomesrs41553319
hgdprs41553319
ensemblrs41553319
gopubmedrs41553319
geneviewrs41553319
scholarrs41553319
googlers41553319
pharmgkbrs41553319
gwascentralrs41553319
openSNPrs41553319
23andMers41553319
23andMe allrs41553319
SNP Nexus

SNPshotrs41553319
SNPdbers41553319
MSV3drs41553319
GWAS Ctlgrs41553319
Max Magnitude0
ClinVar
Risk rs41553319(A,G,T;A,G,T)
Alt rs41553319(A,G,T;A,G,T)
Reference rs41553319(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911127C>A; NC_000006.11:g.29911127C>G; NC_000006.11:g.29911127C>T
CLNSRC
CLNACC