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rs41551916

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41551916(G;T)
Make rs41551916(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271261
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41551916
ebirs41551916
HLIrs41551916
Exacrs41551916
Varsomers41551916
Maprs41551916
PheGenIrs41551916
hapmaprs41551916
1000 genomesrs41551916
hgdprs41551916
ensemblrs41551916
gopubmedrs41551916
geneviewrs41551916
scholarrs41551916
googlers41551916
pharmgkbrs41551916
gwascentralrs41551916
openSNPrs41551916
23andMers41551916
23andMe allrs41551916
SNP Nexus

SNPshotrs41551916
SNPdbers41551916
MSV3drs41551916
GWAS Ctlgrs41551916
Max Magnitude0
ClinVar
Risk rs41551916(T;T)
Alt rs41551916(T;T)
Reference rs41551916(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239038C>A
CLNSRC
CLNACC