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rs786205557

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205557(A;A)
Make rs786205557(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome22
Position41127672
GeneEP300
is asnp
is mentioned by
dbSNPrs786205557
ebirs786205557
HLIrs786205557
Exacrs786205557
Varsomers786205557
Maprs786205557
PheGenIrs786205557
hapmaprs786205557
1000 genomesrs786205557
hgdprs786205557
ensemblrs786205557
gopubmedrs786205557
geneviewrs786205557
scholarrs786205557
googlers786205557
pharmgkbrs786205557
gwascentralrs786205557
openSNPrs786205557
23andMers786205557
23andMe allrs786205557
SNP Nexus

SNPshotrs786205557
SNPdbers786205557
MSV3drs786205557
GWAS Ctlgrs786205557
Max Magnitude0
ClinVar
Risk rs786205557(A;A)
Alt rs786205557(A;A)
Reference rs786205557(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EP300
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.41523676C>A
CLNSRC
CLNACC RCV000171356.1,