Have questions? Visit https://www.reddit.com/r/SNPedia

rs41548914

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41548914(A;A)
Make rs41548914(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356752
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41548914
ebirs41548914
HLIrs41548914
Exacrs41548914
Varsomers41548914
Maprs41548914
PheGenIrs41548914
hapmaprs41548914
1000 genomesrs41548914
hgdprs41548914
ensemblrs41548914
gopubmedrs41548914
geneviewrs41548914
scholarrs41548914
googlers41548914
pharmgkbrs41548914
gwascentralrs41548914
openSNPrs41548914
23andMers41548914
23andMe allrs41548914
SNP Nexus

SNPshotrs41548914
SNPdbers41548914
MSV3drs41548914
GWAS Ctlgrs41548914
Max Magnitude0
ClinVar
Risk rs41548914(A;A) rs41548914(T;T)
Alt rs41548914(A;A) rs41548914(T;T)
Reference Rs41548914(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324529G>A; NC_000006.11:g.31324529G>T
CLNSRC
CLNACC