Have questions? Visit https://www.reddit.com/r/SNPedia

rs41544314

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41544314(A;A)
Make rs41544314(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269239
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41544314
ebirs41544314
HLIrs41544314
Exacrs41544314
Varsomers41544314
Maprs41544314
PheGenIrs41544314
hapmaprs41544314
1000 genomesrs41544314
hgdprs41544314
ensemblrs41544314
gopubmedrs41544314
geneviewrs41544314
scholarrs41544314
googlers41544314
pharmgkbrs41544314
gwascentralrs41544314
openSNPrs41544314
23andMers41544314
23andMe allrs41544314
SNP Nexus

SNPshotrs41544314
SNPdbers41544314
MSV3drs41544314
GWAS Ctlgrs41544314
GMAF0.02709
Max Magnitude0
ClinVar
Risk rs41544314(A;A)
Alt rs41544314(A;A)
Reference rs41544314(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237016C>T
CLNSRC
CLNACC