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

rs1050276

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1050276(A;A)
Make rs1050276(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270291
GeneHLA-C
is asnp
is mentioned by
dbSNPrs1050276
ebirs1050276
HLIrs1050276
Exacrs1050276
Varsomers1050276
Maprs1050276
PheGenIrs1050276
hapmaprs1050276
1000 genomesrs1050276
hgdprs1050276
ensemblrs1050276
gopubmedrs1050276
geneviewrs1050276
scholarrs1050276
googlers1050276
pharmgkbrs1050276
gwascentralrs1050276
openSNPrs1050276
23andMers1050276
23andMe allrs1050276
SNP Nexus

SNPshotrs1050276
SNPdbers1050276
MSV3drs1050276
GWAS Ctlgrs1050276
GMAF0.06795
Max Magnitude0
ClinVar
Risk rs1050276(A;A)
Alt rs1050276(A;A)
Reference rs1050276(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238068C>T
CLNSRC
CLNACC