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

rs67420880

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs67420880(A;C)
Make rs67420880(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271374
GeneHLA-C
is asnp
is mentioned by
dbSNPrs67420880
ebirs67420880
HLIrs67420880
Exacrs67420880
Varsomers67420880
Maprs67420880
PheGenIrs67420880
hapmaprs67420880
1000 genomesrs67420880
hgdprs67420880
ensemblrs67420880
gopubmedrs67420880
geneviewrs67420880
scholarrs67420880
googlers67420880
pharmgkbrs67420880
gwascentralrs67420880
openSNPrs67420880
23andMers67420880
23andMe allrs67420880
SNP Nexus

SNPshotrs67420880
SNPdbers67420880
MSV3drs67420880
GWAS Ctlgrs67420880
GMAF0.2929
Max Magnitude0
ClinVar
Risk rs67420880(C,G;C,G)
Alt rs67420880(C,G;C,G)
Reference rs67420880(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31239151A>C; NC_000006.11:g.31239151A>G
CLNSRC
CLNACC