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rs41560418

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41560418(A;A)
Make rs41560418(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355983
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs41560418
dbSNP (classic)rs41560418
ClinGenrs41560418
ebirs41560418
HLIrs41560418
Exacrs41560418
Gnomadrs41560418
Varsomers41560418
LitVarrs41560418
Maprs41560418
PheGenIrs41560418
Biobankrs41560418
1000 genomesrs41560418
hgdprs41560418
ensemblrs41560418
geneviewrs41560418
scholarrs41560418
googlers41560418
pharmgkbrs41560418
gwascentralrs41560418
openSNPrs41560418
23andMers41560418
SNPshotrs41560418
SNPdbers41560418
MSV3drs41560418
GWAS Ctlgrs41560418
Max Magnitude0
ClinVar
Risk rs41560418(A;A)
Alt rs41560418(A;A)
Reference Rs41560418(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323760C>T
CLNSRC
CLNACC