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rs41549515

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41549515(A;G)
Make rs41549515(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270812
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41549515
ebirs41549515
HLIrs41549515
Exacrs41549515
Varsomers41549515
Maprs41549515
PheGenIrs41549515
hapmaprs41549515
1000 genomesrs41549515
hgdprs41549515
ensemblrs41549515
gopubmedrs41549515
geneviewrs41549515
scholarrs41549515
googlers41549515
pharmgkbrs41549515
gwascentralrs41549515
openSNPrs41549515
23andMers41549515
23andMe allrs41549515
SNP Nexus

SNPshotrs41549515
SNPdbers41549515
MSV3drs41549515
GWAS Ctlgrs41549515
GMAF0.02709
Max Magnitude0
ClinVar
Risk rs41549515(G;G)
Alt rs41549515(G;G)
Reference rs41549515(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238589T>C
CLNSRC
CLNACC