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rs41554814

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41554814(C;T)
Make rs41554814(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271293
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41554814
ebirs41554814
HLIrs41554814
Exacrs41554814
Varsomers41554814
Maprs41554814
PheGenIrs41554814
hapmaprs41554814
1000 genomesrs41554814
hgdprs41554814
ensemblrs41554814
gopubmedrs41554814
geneviewrs41554814
scholarrs41554814
googlers41554814
pharmgkbrs41554814
gwascentralrs41554814
openSNPrs41554814
23andMers41554814
23andMe allrs41554814
SNP Nexus

SNPshotrs41554814
SNPdbers41554814
MSV3drs41554814
GWAS Ctlgrs41554814
Max Magnitude0
ClinVar
Risk rs41554814(T;T)
Alt rs41554814(T;T)
Reference rs41554814(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239070G>A
CLNSRC
CLNACC