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rs41557117

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41557117(A;G)
Make rs41557117(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356238
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41557117
ebirs41557117
HLIrs41557117
Exacrs41557117
Varsomers41557117
Maprs41557117
PheGenIrs41557117
hapmaprs41557117
1000 genomesrs41557117
hgdprs41557117
ensemblrs41557117
gopubmedrs41557117
geneviewrs41557117
scholarrs41557117
googlers41557117
pharmgkbrs41557117
gwascentralrs41557117
openSNPrs41557117
23andMers41557117
23andMe allrs41557117
SNP Nexus

SNPshotrs41557117
SNPdbers41557117
MSV3drs41557117
GWAS Ctlgrs41557117
Max Magnitude0
ClinVar
Risk rs41557117(C,G;C,G)
Alt rs41557117(C,G;C,G)
Reference rs41557117(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324015T>C; NC_000006.11:g.31324015T>G
CLNSRC
CLNACC