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rs41556617

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41556617(A;A)
Make rs41556617(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270009
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41556617
ebirs41556617
HLIrs41556617
Exacrs41556617
Varsomers41556617
Maprs41556617
PheGenIrs41556617
hapmaprs41556617
1000 genomesrs41556617
hgdprs41556617
ensemblrs41556617
gopubmedrs41556617
geneviewrs41556617
scholarrs41556617
googlers41556617
pharmgkbrs41556617
gwascentralrs41556617
openSNPrs41556617
23andMers41556617
23andMe allrs41556617
SNP Nexus

SNPshotrs41556617
SNPdbers41556617
MSV3drs41556617
GWAS Ctlgrs41556617
GMAF0.2429
Max Magnitude0
ClinVar
Risk rs41556617(A;A)
Alt rs41556617(A;A)
Reference rs41556617(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237786A>T
CLNSRC
CLNACC