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rs41562613

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41562613(A;A)
Make rs41562613(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356831
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41562613
ebirs41562613
HLIrs41562613
Exacrs41562613
Varsomers41562613
Maprs41562613
PheGenIrs41562613
hapmaprs41562613
1000 genomesrs41562613
hgdprs41562613
ensemblrs41562613
gopubmedrs41562613
geneviewrs41562613
scholarrs41562613
googlers41562613
pharmgkbrs41562613
gwascentralrs41562613
openSNPrs41562613
23andMers41562613
23andMe allrs41562613
SNP Nexus

SNPshotrs41562613
SNPdbers41562613
MSV3drs41562613
GWAS Ctlgrs41562613
Max Magnitude0
ClinVar
Risk rs41562613(A,G,T;A,G,T)
Alt rs41562613(A,G,T;A,G,T)
Reference rs41562613(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324608G>A; NC_000006.11:g.31324608G>C; NC_000006.11:g.31324608G>T
CLNSRC
CLNACC