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rs41556115

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41556115(A;C)
Make rs41556115(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942980
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41556115
ebirs41556115
HLIrs41556115
Exacrs41556115
Varsomers41556115
Maprs41556115
PheGenIrs41556115
hapmaprs41556115
1000 genomesrs41556115
hgdprs41556115
ensemblrs41556115
gopubmedrs41556115
geneviewrs41556115
scholarrs41556115
googlers41556115
pharmgkbrs41556115
gwascentralrs41556115
openSNPrs41556115
23andMers41556115
23andMe allrs41556115
SNP Nexus

SNPshotrs41556115
SNPdbers41556115
MSV3drs41556115
GWAS Ctlgrs41556115
Max Magnitude0
ClinVar
Risk rs41556115(C,G;C,G)
Alt rs41556115(C,G;C,G)
Reference rs41556115(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910757A>C; NC_000006.11:g.29910757A>G
CLNSRC
CLNACC