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rs41556319

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41556319(C;G)
Make rs41556319(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356005
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41556319
ebirs41556319
HLIrs41556319
Exacrs41556319
Varsomers41556319
Maprs41556319
PheGenIrs41556319
hapmaprs41556319
1000 genomesrs41556319
hgdprs41556319
ensemblrs41556319
gopubmedrs41556319
geneviewrs41556319
scholarrs41556319
googlers41556319
pharmgkbrs41556319
gwascentralrs41556319
openSNPrs41556319
23andMers41556319
23andMe allrs41556319
SNP Nexus

SNPshotrs41556319
SNPdbers41556319
MSV3drs41556319
GWAS Ctlgrs41556319
Max Magnitude0
ClinVar
Risk rs41556319(G;G)
Alt rs41556319(G;G)
Reference rs41556319(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323782G>C
CLNSRC
CLNACC