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

rs3823342

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs3823342(C;C)
Make rs3823342(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29945290
GeneHLA-A
is asnp
is mentioned by
dbSNPrs3823342
dbSNP (classic)rs3823342
ClinGenrs3823342
ebirs3823342
HLIrs3823342
Exacrs3823342
Gnomadrs3823342
Varsomers3823342
LitVarrs3823342
Maprs3823342
PheGenIrs3823342
Biobankrs3823342
1000 genomesrs3823342
hgdprs3823342
ensemblrs3823342
geneviewrs3823342
scholarrs3823342
googlers3823342
pharmgkbrs3823342
gwascentralrs3823342
openSNPrs3823342
23andMers3823342
SNPshotrs3823342
SNPdbers3823342
MSV3drs3823342
GWAS Ctlgrs3823342
GMAF0.4743
Max Magnitude0
? (C;C) (C;T) (T;T) 28


ClinVar
Risk rs3823342(C;C)
Alt rs3823342(C;C)
Reference Rs3823342(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29913067T>C
CLNSRC
CLNACC