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rs41554421

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41554421(A;A)
Make rs41554421(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356787
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs41554421
dbSNP (classic)rs41554421
ClinGenrs41554421
ebirs41554421
HLIrs41554421
Exacrs41554421
Gnomadrs41554421
Varsomers41554421
LitVarrs41554421
Maprs41554421
PheGenIrs41554421
Biobankrs41554421
1000 genomesrs41554421
hgdprs41554421
ensemblrs41554421
geneviewrs41554421
scholarrs41554421
googlers41554421
pharmgkbrs41554421
gwascentralrs41554421
openSNPrs41554421
23andMers41554421
SNPshotrs41554421
SNPdbers41554421
MSV3drs41554421
GWAS Ctlgrs41554421
Max Magnitude0
ClinVar
Risk rs41554421(A;A) rs41554421(C;C) rs41554421(T;T)
Alt rs41554421(A;A) rs41554421(C;C) rs41554421(T;T)
Reference Rs41554421(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324564C>A; NC_000006.11:g.31324564C>G; NC_000006.11:g.31324564C>T
CLNSRC
CLNACC