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rs41542114

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41542114(C;C)
Make rs41542114(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270161
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41542114
ebirs41542114
HLIrs41542114
Exacrs41542114
Varsomers41542114
Maprs41542114
PheGenIrs41542114
hapmaprs41542114
1000 genomesrs41542114
hgdprs41542114
ensemblrs41542114
gopubmedrs41542114
geneviewrs41542114
scholarrs41542114
googlers41542114
pharmgkbrs41542114
gwascentralrs41542114
openSNPrs41542114
23andMers41542114
23andMe allrs41542114
SNP Nexus

SNPshotrs41542114
SNPdbers41542114
MSV3drs41542114
GWAS Ctlgrs41542114
Max Magnitude0
ClinVar
Risk rs41542114(C;C)
Alt rs41542114(C;C)
Reference rs41542114(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237938A>G
CLNSRC
CLNACC