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

rs199474357

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199474357(C;C)
Make rs199474357(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942790
GeneHLA-A
is asnp
is mentioned by
dbSNPrs199474357
ebirs199474357
HLIrs199474357
Exacrs199474357
Varsomers199474357
Maprs199474357
PheGenIrs199474357
hapmaprs199474357
1000 genomesrs199474357
hgdprs199474357
ensemblrs199474357
gopubmedrs199474357
geneviewrs199474357
scholarrs199474357
googlers199474357
pharmgkbrs199474357
gwascentralrs199474357
openSNPrs199474357
23andMers199474357
23andMe allrs199474357
SNP Nexus

SNPshotrs199474357
SNPdbers199474357
MSV3drs199474357
GWAS Ctlgrs199474357
Max Magnitude0
ClinVar
Risk rs199474357(C,G;C,G)
Alt rs199474357(C,G;C,G)
Reference rs199474357(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910567T>C; NC_000006.11:g.29910567T>G
CLNSRC
CLNACC