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rs41553618

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41553618(-;-)
Make rs41553618(-;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356799
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41553618
ebirs41553618
HLIrs41553618
Exacrs41553618
Varsomers41553618
Maprs41553618
PheGenIrs41553618
hapmaprs41553618
1000 genomesrs41553618
hgdprs41553618
ensemblrs41553618
gopubmedrs41553618
geneviewrs41553618
scholarrs41553618
googlers41553618
pharmgkbrs41553618
gwascentralrs41553618
openSNPrs41553618
23andMers41553618
23andMe allrs41553618
SNP Nexus

SNPshotrs41553618
SNPdbers41553618
MSV3drs41553618
GWAS Ctlgrs41553618
Max Magnitude0
ClinVar
Risk rs41553618(;)
Alt rs41553618(;)
Reference rs41553618(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324576delG
CLNSRC
CLNACC