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rs112863520

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs112863520(C;T)
Make rs112863520(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position29945653
GeneHLA-A
is asnp
is mentioned by
dbSNPrs112863520
dbSNP (classic)rs112863520
ClinGenrs112863520
ebirs112863520
HLIrs112863520
Exacrs112863520
Gnomadrs112863520
Varsomers112863520
LitVarrs112863520
Maprs112863520
PheGenIrs112863520
Biobankrs112863520
1000 genomesrs112863520
hgdprs112863520
ensemblrs112863520
geneviewrs112863520
scholarrs112863520
googlers112863520
pharmgkbrs112863520
gwascentralrs112863520
openSNPrs112863520
23andMers112863520
SNPshotrs112863520
SNPdbers112863520
MSV3drs112863520
GWAS Ctlgrs112863520
GMAF0.1616
Max Magnitude0
ClinVar
Risk rs112863520(T;T)
Alt rs112863520(T;T)
Reference Rs112863520(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29913430C; NC_000006.11:g.29913430C>T
CLNSRC
CLNACC