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rs41544212

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41544212(C;C)
Make rs41544212(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271038
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41544212
ebirs41544212
HLIrs41544212
Exacrs41544212
Varsomers41544212
Maprs41544212
PheGenIrs41544212
hapmaprs41544212
1000 genomesrs41544212
hgdprs41544212
ensemblrs41544212
gopubmedrs41544212
geneviewrs41544212
scholarrs41544212
googlers41544212
pharmgkbrs41544212
gwascentralrs41544212
openSNPrs41544212
23andMers41544212
23andMe allrs41544212
SNP Nexus

SNPshotrs41544212
SNPdbers41544212
MSV3drs41544212
GWAS Ctlgrs41544212
GMAF0.2016
Max Magnitude0
ClinVar
Risk rs41544212(C;C)
Alt rs41544212(C;C)
Reference rs41544212(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238815A>G
CLNSRC
CLNACC