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rs41551317

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41551317(A;A)
Make rs41551317(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943455
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41551317
dbSNP (classic)rs41551317
ClinGenrs41551317
ebirs41551317
HLIrs41551317
Exacrs41551317
Gnomadrs41551317
Varsomers41551317
LitVarrs41551317
Maprs41551317
PheGenIrs41551317
Biobankrs41551317
1000 genomesrs41551317
hgdprs41551317
ensemblrs41551317
geneviewrs41551317
scholarrs41551317
googlers41551317
pharmgkbrs41551317
gwascentralrs41551317
openSNPrs41551317
23andMers41551317
SNPshotrs41551317
SNPdbers41551317
MSV3drs41551317
GWAS Ctlgrs41551317
Max Magnitude0
ClinVar
Risk rs41551317(A;A) rs41551317(C;C)
Alt rs41551317(A;A) rs41551317(C;C)
Reference Rs41551317(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911232G>A; NC_000006.11:g.29911232G>C
CLNSRC
CLNACC