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rs78306866

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs78306866(C;C)
Make rs78306866(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942965
GeneHLA-A
is asnp
is mentioned by
dbSNPrs78306866
ebirs78306866
HLIrs78306866
Exacrs78306866
Varsomers78306866
Maprs78306866
PheGenIrs78306866
hapmaprs78306866
1000 genomesrs78306866
hgdprs78306866
ensemblrs78306866
gopubmedrs78306866
geneviewrs78306866
scholarrs78306866
googlers78306866
pharmgkbrs78306866
gwascentralrs78306866
openSNPrs78306866
23andMers78306866
23andMe allrs78306866
SNP Nexus

SNPshotrs78306866
SNPdbers78306866
MSV3drs78306866
GWAS Ctlgrs78306866
GMAF0.3444
Max Magnitude0
ClinVar
Risk rs78306866(C,T;C,T)
Alt rs78306866(C,T;C,T)
Reference rs78306866(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910742G; NC_000006.11:g.29910742G>C; NC_000006.11:g.29910742G>T
CLNSRC
CLNACC