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rs41544316

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41544316(C;G)
Make rs41544316(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943025
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41544316
ebirs41544316
HLIrs41544316
Exacrs41544316
Varsomers41544316
Maprs41544316
PheGenIrs41544316
hapmaprs41544316
1000 genomesrs41544316
hgdprs41544316
ensemblrs41544316
gopubmedrs41544316
geneviewrs41544316
scholarrs41544316
googlers41544316
pharmgkbrs41544316
gwascentralrs41544316
openSNPrs41544316
23andMers41544316
23andMe allrs41544316
SNP Nexus

SNPshotrs41544316
SNPdbers41544316
MSV3drs41544316
GWAS Ctlgrs41544316
Max Magnitude0
ClinVar
Risk rs41544316(A,G,T;A,G,T)
Alt rs41544316(A,G,T;A,G,T)
Reference rs41544316(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910802C>A; NC_000006.11:g.29910802C>G; NC_000006.11:g.29910802C>T
CLNSRC
CLNACC