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rs17878860

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs17878860(A;G)
Make rs17878860(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943583
GeneHLA-A
is asnp
is mentioned by
dbSNPrs17878860
dbSNP (classic)rs17878860
ClinGenrs17878860
ebirs17878860
HLIrs17878860
Exacrs17878860
Gnomadrs17878860
Varsomers17878860
LitVarrs17878860
Maprs17878860
PheGenIrs17878860
Biobankrs17878860
1000 genomesrs17878860
hgdprs17878860
ensemblrs17878860
geneviewrs17878860
scholarrs17878860
googlers17878860
pharmgkbrs17878860
gwascentralrs17878860
openSNPrs17878860
23andMers17878860
SNPshotrs17878860
SNPdbers17878860
MSV3drs17878860
GWAS Ctlgrs17878860
GMAF0.1515
Max Magnitude0
ClinVar
Risk rs17878860(G;G)
Alt rs17878860(G;G)
Reference Rs17878860(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911360A>G
CLNSRC
CLNACC