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rs41552017

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41552017(-;-)
Make rs41552017(-;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355748
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41552017
ebirs41552017
HLIrs41552017
Exacrs41552017
Varsomers41552017
Maprs41552017
PheGenIrs41552017
hapmaprs41552017
1000 genomesrs41552017
hgdprs41552017
ensemblrs41552017
gopubmedrs41552017
geneviewrs41552017
scholarrs41552017
googlers41552017
pharmgkbrs41552017
gwascentralrs41552017
openSNPrs41552017
23andMers41552017
23andMe allrs41552017
SNP Nexus

SNPshotrs41552017
SNPdbers41552017
MSV3drs41552017
GWAS Ctlgrs41552017
Max Magnitude0
ClinVar
Risk rs41552017(;)
Alt rs41552017(;)
Reference rs41552017(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323525delC
CLNSRC
CLNACC