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rs41557212

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41557212(A;C)
Make rs41557212(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943343
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41557212
ebirs41557212
HLIrs41557212
Exacrs41557212
Varsomers41557212
Maprs41557212
PheGenIrs41557212
hapmaprs41557212
1000 genomesrs41557212
hgdprs41557212
ensemblrs41557212
gopubmedrs41557212
geneviewrs41557212
scholarrs41557212
googlers41557212
pharmgkbrs41557212
gwascentralrs41557212
openSNPrs41557212
23andMers41557212
23andMe allrs41557212
SNP Nexus

SNPshotrs41557212
SNPdbers41557212
MSV3drs41557212
GWAS Ctlgrs41557212
Max Magnitude0
ClinVar
Risk rs41557212(C,G,T;C,G,T)
Alt rs41557212(C,G,T;C,G,T)
Reference rs41557212(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911120A>C; NC_000006.11:g.29911120A>G; NC_000006.11:g.29911120A>T
CLNSRC
CLNACC