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rs41544716

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41544716(-;-)
Make rs41544716(-;A)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269339
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41544716
ebirs41544716
HLIrs41544716
Exacrs41544716
Varsomers41544716
Maprs41544716
PheGenIrs41544716
hapmaprs41544716
1000 genomesrs41544716
hgdprs41544716
ensemblrs41544716
gopubmedrs41544716
geneviewrs41544716
scholarrs41544716
googlers41544716
pharmgkbrs41544716
gwascentralrs41544716
openSNPrs41544716
23andMers41544716
23andMe allrs41544716
SNP Nexus

SNPshotrs41544716
SNPdbers41544716
MSV3drs41544716
GWAS Ctlgrs41544716
Max Magnitude0
ClinVar
Risk rs41544716(;)
Alt rs41544716(;)
Reference rs41544716(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237116delT
CLNSRC
CLNACC