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rs41556412

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41556412(-;-)
Make rs41556412(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324754
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41556412
ebirs41556412
HLIrs41556412
Exacrs41556412
Varsomers41556412
Maprs41556412
PheGenIrs41556412
hapmaprs41556412
1000 genomesrs41556412
hgdprs41556412
ensemblrs41556412
gopubmedrs41556412
geneviewrs41556412
scholarrs41556412
googlers41556412
pharmgkbrs41556412
gwascentralrs41556412
openSNPrs41556412
23andMers41556412
23andMe allrs41556412
SNP Nexus

SNPshotrs41556412
SNPdbers41556412
MSV3drs41556412
GWAS Ctlgrs41556412
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41556412(;)
Alt rs41556412(;)
Reference rs41556412(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324754delG
CLNSRC
CLNACC