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rs41563818

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41563818(C;T)
Make rs41563818(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355637
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41563818
ebirs41563818
HLIrs41563818
Exacrs41563818
Varsomers41563818
Maprs41563818
PheGenIrs41563818
hapmaprs41563818
1000 genomesrs41563818
hgdprs41563818
ensemblrs41563818
gopubmedrs41563818
geneviewrs41563818
scholarrs41563818
googlers41563818
pharmgkbrs41563818
gwascentralrs41563818
openSNPrs41563818
23andMers41563818
23andMe allrs41563818
SNP Nexus

SNPshotrs41563818
SNPdbers41563818
MSV3drs41563818
GWAS Ctlgrs41563818
GMAF0.03306
Max Magnitude0
ClinVar
Risk rs41563818(T;T)
Alt rs41563818(T;T)
Reference rs41563818(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323414G>A
CLNSRC
CLNACC