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rs41557818

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41557818(A;A)
Make rs41557818(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356231
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41557818
ebirs41557818
HLIrs41557818
Exacrs41557818
Varsomers41557818
Maprs41557818
PheGenIrs41557818
hapmaprs41557818
1000 genomesrs41557818
hgdprs41557818
ensemblrs41557818
gopubmedrs41557818
geneviewrs41557818
scholarrs41557818
googlers41557818
pharmgkbrs41557818
gwascentralrs41557818
openSNPrs41557818
23andMers41557818
23andMe allrs41557818
SNP Nexus

SNPshotrs41557818
SNPdbers41557818
MSV3drs41557818
GWAS Ctlgrs41557818
Max Magnitude0
ClinVar
Risk rs41557818(A,C;A,C)
Alt rs41557818(A,C;A,C)
Reference rs41557818(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324008C>G; NC_000006.11:g.31324008C>T
CLNSRC
CLNACC