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rs67827555

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs67827555(C;C)
Make rs67827555(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269576
GeneHLA-C
is asnp
is mentioned by
dbSNPrs67827555
ebirs67827555
HLIrs67827555
Exacrs67827555
Varsomers67827555
Maprs67827555
PheGenIrs67827555
hapmaprs67827555
1000 genomesrs67827555
hgdprs67827555
ensemblrs67827555
gopubmedrs67827555
geneviewrs67827555
scholarrs67827555
googlers67827555
pharmgkbrs67827555
gwascentralrs67827555
openSNPrs67827555
23andMers67827555
23andMe allrs67827555
SNP Nexus

SNPshotrs67827555
SNPdbers67827555
MSV3drs67827555
GWAS Ctlgrs67827555
GMAF0.2236
Max Magnitude0
ClinVar
Risk rs67827555(C;C)
Alt rs67827555(C;C)
Reference rs67827555(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31237353T>C
CLNSRC
CLNACC