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

rs41545513

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41545513(C;C)
Make rs41545513(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944392
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41545513
dbSNP (classic)rs41545513
ClinGenrs41545513
ebirs41545513
HLIrs41545513
Exacrs41545513
Gnomadrs41545513
Varsomers41545513
LitVarrs41545513
Maprs41545513
PheGenIrs41545513
Biobankrs41545513
1000 genomesrs41545513
hgdprs41545513
ensemblrs41545513
geneviewrs41545513
scholarrs41545513
googlers41545513
pharmgkbrs41545513
gwascentralrs41545513
openSNPrs41545513
23andMers41545513
SNPshotrs41545513
SNPdbers41545513
MSV3drs41545513
GWAS Ctlgrs41545513
Max Magnitude0
ClinVar
Risk rs41545513(A;A) rs41545513(C;C)
Alt rs41545513(A;A) rs41545513(C;C)
Reference Rs41545513(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912169G>A
CLNSRC
CLNACC