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rs281864764

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281864764(C;C)
Make rs281864764(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944160
GeneHLA-A
is asnp
is mentioned by
dbSNPrs281864764
ClinGenrs281864764
ebirs281864764
HLIrs281864764
Exacrs281864764
Varsomers281864764
Maprs281864764
PheGenIrs281864764
hapmaprs281864764
1000 genomesrs281864764
hgdprs281864764
ensemblrs281864764
gopubmedrs281864764
geneviewrs281864764
scholarrs281864764
googlers281864764
pharmgkbrs281864764
gwascentralrs281864764
openSNPrs281864764
23andMers281864764
23andMe allrs281864764
SNP Nexus

SNPshotrs281864764
SNPdbers281864764
MSV3drs281864764
GWAS Ctlgrs281864764
Max Magnitude0
ClinVar
Risk rs281864764(C;C)
Alt rs281864764(C;C)
Reference Rs281864764(G;G)
Significance Non-pathogenic
Disease Abnormality of neuronal migration
Variation info
Gene HLA-A
CLNDBN Abnormality of neuronal migration
Reversed 0
HGVS NC_000006.11:g.29911937G>C
CLNSRC
CLNACC RCV000201406.1,