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rs41551016

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41551016(A;A)
Make rs41551016(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271163
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41551016
ebirs41551016
HLIrs41551016
Exacrs41551016
Varsomers41551016
Maprs41551016
PheGenIrs41551016
hapmaprs41551016
1000 genomesrs41551016
hgdprs41551016
ensemblrs41551016
gopubmedrs41551016
geneviewrs41551016
scholarrs41551016
googlers41551016
pharmgkbrs41551016
gwascentralrs41551016
openSNPrs41551016
23andMers41551016
23andMe allrs41551016
SNP Nexus

SNPshotrs41551016
SNPdbers41551016
MSV3drs41551016
GWAS Ctlgrs41551016
Max Magnitude0
ClinVar
Risk rs41551016(A;A)
Alt rs41551016(A;A)
Reference rs41551016(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238940C>T
CLNSRC
CLNACC