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rs41551612

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41551612(C;T)
Make rs41551612(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944248
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41551612
ebirs41551612
HLIrs41551612
Exacrs41551612
Varsomers41551612
Maprs41551612
PheGenIrs41551612
hapmaprs41551612
1000 genomesrs41551612
hgdprs41551612
ensemblrs41551612
gopubmedrs41551612
geneviewrs41551612
scholarrs41551612
googlers41551612
pharmgkbrs41551612
gwascentralrs41551612
openSNPrs41551612
23andMers41551612
23andMe allrs41551612
SNP Nexus

SNPshotrs41551612
SNPdbers41551612
MSV3drs41551612
GWAS Ctlgrs41551612
Max Magnitude0
ClinVar
Risk rs41551612(T;T)
Alt rs41551612(T;T)
Reference rs41551612(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912025C>T
CLNSRC
CLNACC