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rs41548616

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41548616(C;T)
Make rs41548616(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356872
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41548616
ebirs41548616
HLIrs41548616
Exacrs41548616
Varsomers41548616
Maprs41548616
PheGenIrs41548616
hapmaprs41548616
1000 genomesrs41548616
hgdprs41548616
ensemblrs41548616
gopubmedrs41548616
geneviewrs41548616
scholarrs41548616
googlers41548616
pharmgkbrs41548616
gwascentralrs41548616
openSNPrs41548616
23andMers41548616
23andMe allrs41548616
SNP Nexus

SNPshotrs41548616
SNPdbers41548616
MSV3drs41548616
GWAS Ctlgrs41548616
Max Magnitude0
ClinVar
Risk rs41548616(T;T)
Alt rs41548616(T;T)
Reference rs41548616(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324649G>A
CLNSRC
CLNACC