Have questions? Visit https://www.reddit.com/r/SNPedia

rs41557913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41557913(A;G)
Make rs41557913(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943540
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41557913
ebirs41557913
HLIrs41557913
Exacrs41557913
Varsomers41557913
Maprs41557913
PheGenIrs41557913
hapmaprs41557913
1000 genomesrs41557913
hgdprs41557913
ensemblrs41557913
gopubmedrs41557913
geneviewrs41557913
scholarrs41557913
googlers41557913
pharmgkbrs41557913
gwascentralrs41557913
openSNPrs41557913
23andMers41557913
23andMe allrs41557913
SNP Nexus

SNPshotrs41557913
SNPdbers41557913
MSV3drs41557913
GWAS Ctlgrs41557913
Max Magnitude0
ClinVar
Risk rs41557913(G,T;G,T)
Alt rs41557913(G,T;G,T)
Reference rs41557913(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911317A>G; NC_000006.11:g.29911317A>T
CLNSRC
CLNACC