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rs41557613

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41557613(A;A)
Make rs41557613(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942877
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41557613
ebirs41557613
HLIrs41557613
Exacrs41557613
Varsomers41557613
Maprs41557613
PheGenIrs41557613
hapmaprs41557613
1000 genomesrs41557613
hgdprs41557613
ensemblrs41557613
gopubmedrs41557613
geneviewrs41557613
scholarrs41557613
googlers41557613
pharmgkbrs41557613
gwascentralrs41557613
openSNPrs41557613
23andMers41557613
23andMe allrs41557613
SNP Nexus

SNPshotrs41557613
SNPdbers41557613
MSV3drs41557613
GWAS Ctlgrs41557613
Max Magnitude0
ClinVar
Risk rs41557613(A,G,T;A,G,T)
Alt rs41557613(A,G,T;A,G,T)
Reference rs41557613(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910654C>A; NC_000006.11:g.29910654C>G; NC_000006.11:g.29910654C>T
CLNSRC
CLNACC