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

rs12721827

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs12721827(C;T)
Make rs12721827(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356433
GeneHLA-B
is asnp
is mentioned by
dbSNPrs12721827
ebirs12721827
HLIrs12721827
Exacrs12721827
Varsomers12721827
Maprs12721827
PheGenIrs12721827
hapmaprs12721827
1000 genomesrs12721827
hgdprs12721827
ensemblrs12721827
gopubmedrs12721827
geneviewrs12721827
scholarrs12721827
googlers12721827
pharmgkbrs12721827
gwascentralrs12721827
openSNPrs12721827
23andMers12721827
23andMe allrs12721827
SNP Nexus

SNPshotrs12721827
SNPdbers12721827
MSV3drs12721827
GWAS Ctlgrs12721827
GMAF0.2511
Max Magnitude0
ClinVar
Risk rs12721827(A,G,T;A,G,T)
Alt rs12721827(A,G,T;A,G,T)
Reference rs12721827(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324210G>A; NC_000006.11:g.31324210G>C; NC_000006.11:g.31324210G>T
CLNSRC
CLNACC