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rs41557719

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41557719(C;T)
Make rs41557719(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944490
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41557719
ebirs41557719
HLIrs41557719
Exacrs41557719
Varsomers41557719
Maprs41557719
PheGenIrs41557719
hapmaprs41557719
1000 genomesrs41557719
hgdprs41557719
ensemblrs41557719
gopubmedrs41557719
geneviewrs41557719
scholarrs41557719
googlers41557719
pharmgkbrs41557719
gwascentralrs41557719
openSNPrs41557719
23andMers41557719
23andMe allrs41557719
SNP Nexus

SNPshotrs41557719
SNPdbers41557719
MSV3drs41557719
GWAS Ctlgrs41557719
Max Magnitude0
ClinVar
Risk rs41557719(T;T)
Alt rs41557719(T;T)
Reference rs41557719(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912267C>T
CLNSRC
CLNACC