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rs78545099

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs78545099(A;G)
Make rs78545099(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356708
GeneHLA-B
is asnp
is mentioned by
dbSNPrs78545099
ebirs78545099
HLIrs78545099
Exacrs78545099
Varsomers78545099
Maprs78545099
PheGenIrs78545099
hapmaprs78545099
1000 genomesrs78545099
hgdprs78545099
ensemblrs78545099
gopubmedrs78545099
geneviewrs78545099
scholarrs78545099
googlers78545099
pharmgkbrs78545099
gwascentralrs78545099
openSNPrs78545099
23andMers78545099
23andMe allrs78545099
SNP Nexus

SNPshotrs78545099
SNPdbers78545099
MSV3drs78545099
GWAS Ctlgrs78545099
Max Magnitude0
ClinVar
Risk rs78545099(C,G,T;C,G,T)
Alt rs78545099(C,G,T;C,G,T)
Reference rs78545099(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324485T>A; NC_000006.11:g.31324485T>C; NC_000006.11:g.31324485T>G
CLNSRC
CLNACC