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rs41560117

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41560117(A;T)
Make rs41560117(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356783
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41560117
ebirs41560117
HLIrs41560117
Exacrs41560117
Varsomers41560117
Maprs41560117
PheGenIrs41560117
hapmaprs41560117
1000 genomesrs41560117
hgdprs41560117
ensemblrs41560117
gopubmedrs41560117
geneviewrs41560117
scholarrs41560117
googlers41560117
pharmgkbrs41560117
gwascentralrs41560117
openSNPrs41560117
23andMers41560117
23andMe allrs41560117
SNP Nexus

SNPshotrs41560117
SNPdbers41560117
MSV3drs41560117
GWAS Ctlgrs41560117
Max Magnitude0
ClinVar
Risk rs41560117(T;T)
Alt rs41560117(T;T)
Reference rs41560117(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324560T>A
CLNSRC
CLNACC