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rs41552221

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41552221(A;A)
Make rs41552221(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356455
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs41552221
dbSNP (classic)rs41552221
ClinGenrs41552221
ebirs41552221
HLIrs41552221
Exacrs41552221
Gnomadrs41552221
Varsomers41552221
LitVarrs41552221
Maprs41552221
PheGenIrs41552221
Biobankrs41552221
1000 genomesrs41552221
hgdprs41552221
ensemblrs41552221
geneviewrs41552221
scholarrs41552221
googlers41552221
pharmgkbrs41552221
gwascentralrs41552221
openSNPrs41552221
23andMers41552221
SNPshotrs41552221
SNPdbers41552221
MSV3drs41552221
GWAS Ctlgrs41552221
Max Magnitude0
ClinVar
Risk rs41552221(A;A)
Alt rs41552221(A;A)
Reference Rs41552221(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324232C>T
CLNSRC
CLNACC