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rs41548614

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41548614(G;T)
Make rs41548614(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942568
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41548614
ebirs41548614
HLIrs41548614
Exacrs41548614
Varsomers41548614
Maprs41548614
PheGenIrs41548614
hapmaprs41548614
1000 genomesrs41548614
hgdprs41548614
ensemblrs41548614
gopubmedrs41548614
geneviewrs41548614
scholarrs41548614
googlers41548614
pharmgkbrs41548614
gwascentralrs41548614
openSNPrs41548614
23andMers41548614
23andMe allrs41548614
SNP Nexus

SNPshotrs41548614
SNPdbers41548614
MSV3drs41548614
GWAS Ctlgrs41548614
Max Magnitude0
ClinVar
Risk rs41548614(T;T)
Alt rs41548614(T;T)
Reference rs41548614(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910345G>T
CLNSRC
CLNACC