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rs41549919

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41549919(A;A)
Make rs41549919(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271627
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41549919
ebirs41549919
HLIrs41549919
Exacrs41549919
Varsomers41549919
Maprs41549919
PheGenIrs41549919
hapmaprs41549919
1000 genomesrs41549919
hgdprs41549919
ensemblrs41549919
gopubmedrs41549919
geneviewrs41549919
scholarrs41549919
googlers41549919
pharmgkbrs41549919
gwascentralrs41549919
openSNPrs41549919
23andMers41549919
23andMe allrs41549919
SNP Nexus

SNPshotrs41549919
SNPdbers41549919
MSV3drs41549919
GWAS Ctlgrs41549919
Max Magnitude0
ClinVar
Risk rs41549919(A;A)
Alt rs41549919(A;A)
Reference rs41549919(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239404C>T
CLNSRC
CLNACC