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rs41560617

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41560617(C;C)
Make rs41560617(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269984
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41560617
ebirs41560617
HLIrs41560617
Exacrs41560617
Varsomers41560617
Maprs41560617
PheGenIrs41560617
hapmaprs41560617
1000 genomesrs41560617
hgdprs41560617
ensemblrs41560617
gopubmedrs41560617
geneviewrs41560617
scholarrs41560617
googlers41560617
pharmgkbrs41560617
gwascentralrs41560617
openSNPrs41560617
23andMers41560617
23andMe allrs41560617
SNP Nexus

SNPshotrs41560617
SNPdbers41560617
MSV3drs41560617
GWAS Ctlgrs41560617
GMAF0.01882
Max Magnitude0
ClinVar
Risk rs41560617(C;C)
Alt rs41560617(C;C)
Reference rs41560617(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237761A>G
CLNSRC
CLNACC