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rs41561714

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41561714(A;A)
Make rs41561714(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943317
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41561714
ebirs41561714
HLIrs41561714
Exacrs41561714
Varsomers41561714
Maprs41561714
PheGenIrs41561714
hapmaprs41561714
1000 genomesrs41561714
hgdprs41561714
ensemblrs41561714
gopubmedrs41561714
geneviewrs41561714
scholarrs41561714
googlers41561714
pharmgkbrs41561714
gwascentralrs41561714
openSNPrs41561714
23andMers41561714
23andMe allrs41561714
SNP Nexus

SNPshotrs41561714
SNPdbers41561714
MSV3drs41561714
GWAS Ctlgrs41561714
Max Magnitude0
ClinVar
Risk rs41561714(A,C,T;A,C,T)
Alt rs41561714(A,C,T;A,C,T)
Reference rs41561714(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911094G>A; NC_000006.11:g.29911094G>C; NC_000006.11:g.29911094G>T
CLNSRC
CLNACC