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rs41552717

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41552717(A;A)
Make rs41552717(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356845
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41552717
ebirs41552717
HLIrs41552717
Exacrs41552717
Varsomers41552717
Maprs41552717
PheGenIrs41552717
hapmaprs41552717
1000 genomesrs41552717
hgdprs41552717
ensemblrs41552717
gopubmedrs41552717
geneviewrs41552717
scholarrs41552717
googlers41552717
pharmgkbrs41552717
gwascentralrs41552717
openSNPrs41552717
23andMers41552717
23andMe allrs41552717
SNP Nexus

SNPshotrs41552717
SNPdbers41552717
MSV3drs41552717
GWAS Ctlgrs41552717
Max Magnitude0
ClinVar
Risk rs41552717(A,G;A,G)
Alt rs41552717(A,G;A,G)
Reference rs41552717(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324622G>C; NC_000006.11:g.31324622G>T
CLNSRC
CLNACC