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rs41560716

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41560716(A;T)
Make rs41560716(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271342
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41560716
ebirs41560716
HLIrs41560716
Exacrs41560716
Varsomers41560716
Maprs41560716
PheGenIrs41560716
hapmaprs41560716
1000 genomesrs41560716
hgdprs41560716
ensemblrs41560716
gopubmedrs41560716
geneviewrs41560716
scholarrs41560716
googlers41560716
pharmgkbrs41560716
gwascentralrs41560716
openSNPrs41560716
23andMers41560716
23andMe allrs41560716
SNP Nexus

SNPshotrs41560716
SNPdbers41560716
MSV3drs41560716
GWAS Ctlgrs41560716
Max Magnitude0
ClinVar
Risk rs41560716(T;T)
Alt rs41560716(T;T)
Reference rs41560716(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239119T>A
CLNSRC
CLNACC