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

rs78674188

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs78674188(A;C)
Make rs78674188(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943460
GeneHLA-A
is asnp
is mentioned by
dbSNPrs78674188
ebirs78674188
HLIrs78674188
Exacrs78674188
Varsomers78674188
Maprs78674188
PheGenIrs78674188
hapmaprs78674188
1000 genomesrs78674188
hgdprs78674188
ensemblrs78674188
gopubmedrs78674188
geneviewrs78674188
scholarrs78674188
googlers78674188
pharmgkbrs78674188
gwascentralrs78674188
openSNPrs78674188
23andMers78674188
23andMe allrs78674188
SNP Nexus

SNPshotrs78674188
SNPdbers78674188
MSV3drs78674188
GWAS Ctlgrs78674188
Max Magnitude0
ClinVar
Risk rs78674188(C,G;C,G)
Alt rs78674188(C,G;C,G)
Reference rs78674188(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911237A>C; NC_000006.11:g.29911237A>G
CLNSRC
CLNACC