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rs41546215

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41546215(A;A)
Make rs41546215(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271307
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41546215
ebirs41546215
HLIrs41546215
Exacrs41546215
Varsomers41546215
Maprs41546215
PheGenIrs41546215
hapmaprs41546215
1000 genomesrs41546215
hgdprs41546215
ensemblrs41546215
gopubmedrs41546215
geneviewrs41546215
scholarrs41546215
googlers41546215
pharmgkbrs41546215
gwascentralrs41546215
openSNPrs41546215
23andMers41546215
23andMe allrs41546215
SNP Nexus

SNPshotrs41546215
SNPdbers41546215
MSV3drs41546215
GWAS Ctlgrs41546215
Max Magnitude0
ClinVar
Risk rs41546215(A,T;A,T)
Alt rs41546215(A,T;A,T)
Reference rs41546215(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239084G>A; NC_000006.11:g.31239084G>T
CLNSRC
CLNACC