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rs41557815

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41557815(A;A)
Make rs41557815(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942925
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41557815
ebirs41557815
HLIrs41557815
Exacrs41557815
Varsomers41557815
Maprs41557815
PheGenIrs41557815
hapmaprs41557815
1000 genomesrs41557815
hgdprs41557815
ensemblrs41557815
gopubmedrs41557815
geneviewrs41557815
scholarrs41557815
googlers41557815
pharmgkbrs41557815
gwascentralrs41557815
openSNPrs41557815
23andMers41557815
23andMe allrs41557815
SNP Nexus

SNPshotrs41557815
SNPdbers41557815
MSV3drs41557815
GWAS Ctlgrs41557815
Max Magnitude0
ClinVar
Risk rs41557815(A,G,T;A,G,T)
Alt rs41557815(A,G,T;A,G,T)
Reference rs41557815(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910702C>A; NC_000006.11:g.29910702C>G; NC_000006.11:g.29910702C>T
CLNSRC
CLNACC