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

rs11547351

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11547351(A;A)
Make rs11547351(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271646
GeneHLA-C
is asnp
is mentioned by
dbSNPrs11547351
ebirs11547351
HLIrs11547351
Exacrs11547351
Varsomers11547351
Maprs11547351
PheGenIrs11547351
hapmaprs11547351
1000 genomesrs11547351
hgdprs11547351
ensemblrs11547351
gopubmedrs11547351
geneviewrs11547351
scholarrs11547351
googlers11547351
pharmgkbrs11547351
gwascentralrs11547351
openSNPrs11547351
23andMers11547351
23andMe allrs11547351
SNP Nexus

SNPshotrs11547351
SNPdbers11547351
MSV3drs11547351
GWAS Ctlgrs11547351
Max Magnitude0
ClinVar
Risk rs11547351(A,C;A,C)
Alt rs11547351(A,C;A,C)
Reference rs11547351(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239423C>G; NC_000006.11:g.31239423C>T
CLNSRC
CLNACC