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rs41563914

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41563914(A;A)
Make rs41563914(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356332
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41563914
ebirs41563914
HLIrs41563914
Exacrs41563914
Varsomers41563914
Maprs41563914
PheGenIrs41563914
hapmaprs41563914
1000 genomesrs41563914
hgdprs41563914
ensemblrs41563914
gopubmedrs41563914
geneviewrs41563914
scholarrs41563914
googlers41563914
pharmgkbrs41563914
gwascentralrs41563914
openSNPrs41563914
23andMers41563914
23andMe allrs41563914
SNP Nexus

SNPshotrs41563914
SNPdbers41563914
MSV3drs41563914
GWAS Ctlgrs41563914
Max Magnitude0
ClinVar
Risk rs41563914(A,C,T;A,C,T)
Alt rs41563914(A,C,T;A,C,T)
Reference rs41563914(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324109C>A; NC_000006.11:g.31324109C>G; NC_000006.11:g.31324109C>T
CLNSRC
CLNACC