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rs41560613

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41560613(A;A)
Make rs41560613(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356223
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41560613
ebirs41560613
HLIrs41560613
Exacrs41560613
Varsomers41560613
Maprs41560613
PheGenIrs41560613
hapmaprs41560613
1000 genomesrs41560613
hgdprs41560613
ensemblrs41560613
gopubmedrs41560613
geneviewrs41560613
scholarrs41560613
googlers41560613
pharmgkbrs41560613
gwascentralrs41560613
openSNPrs41560613
23andMers41560613
23andMe allrs41560613
SNP Nexus

SNPshotrs41560613
SNPdbers41560613
MSV3drs41560613
GWAS Ctlgrs41560613
Max Magnitude0
ClinVar
Risk rs41560613(A,T;A,T)
Alt rs41560613(A,T;A,T)
Reference rs41560613(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324000C>A; NC_000006.11:g.31324000C>T
CLNSRC
CLNACC