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rs41550613

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41550613(A;A)
Make rs41550613(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271107
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41550613
ebirs41550613
HLIrs41550613
Exacrs41550613
Varsomers41550613
Maprs41550613
PheGenIrs41550613
hapmaprs41550613
1000 genomesrs41550613
hgdprs41550613
ensemblrs41550613
gopubmedrs41550613
geneviewrs41550613
scholarrs41550613
googlers41550613
pharmgkbrs41550613
gwascentralrs41550613
openSNPrs41550613
23andMers41550613
23andMe allrs41550613
SNP Nexus

SNPshotrs41550613
SNPdbers41550613
MSV3drs41550613
GWAS Ctlgrs41550613
Max Magnitude0
ClinVar
Risk rs41550613(A;A)
Alt rs41550613(A;A)
Reference rs41550613(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238884G>T
CLNSRC
CLNACC