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rs41562515

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41562515(A;A)
Make rs41562515(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942977
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41562515
ClinGenrs41562515
ebirs41562515
HLIrs41562515
Exacrs41562515
Varsomers41562515
Maprs41562515
PheGenIrs41562515
hapmaprs41562515
1000 genomesrs41562515
hgdprs41562515
ensemblrs41562515
gopubmedrs41562515
geneviewrs41562515
scholarrs41562515
googlers41562515
pharmgkbrs41562515
gwascentralrs41562515
openSNPrs41562515
23andMers41562515
23andMe allrs41562515
SNP Nexus

SNPshotrs41562515
SNPdbers41562515
MSV3drs41562515
GWAS Ctlgrs41562515
Max Magnitude0
ClinVar
Risk rs41562515(A;A) rs41562515(T;T)
Alt rs41562515(A;A) rs41562515(T;T)
Reference Rs41562515(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910754C>A; NC_000006.11:g.29910754C>T
CLNSRC
CLNACC