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rs41564314

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41564314(A;A)
Make rs41564314(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271318
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41564314
ebirs41564314
HLIrs41564314
Exacrs41564314
Varsomers41564314
Maprs41564314
PheGenIrs41564314
hapmaprs41564314
1000 genomesrs41564314
hgdprs41564314
ensemblrs41564314
gopubmedrs41564314
geneviewrs41564314
scholarrs41564314
googlers41564314
pharmgkbrs41564314
gwascentralrs41564314
openSNPrs41564314
23andMers41564314
23andMe allrs41564314
SNP Nexus

SNPshotrs41564314
SNPdbers41564314
MSV3drs41564314
GWAS Ctlgrs41564314
Max Magnitude0
ClinVar
Risk rs41564314(A;A)
Alt rs41564314(A;A)
Reference rs41564314(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239095C>T
CLNSRC
CLNACC