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rs587783510

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783510(C;T)
Make rs587783510(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome16
Position3728959
GeneCREBBP
is asnp
is mentioned by
dbSNPrs587783510
ebirs587783510
HLIrs587783510
Exacrs587783510
Varsomers587783510
Maprs587783510
PheGenIrs587783510
hapmaprs587783510
1000 genomesrs587783510
hgdprs587783510
ensemblrs587783510
gopubmedrs587783510
geneviewrs587783510
scholarrs587783510
googlers587783510
pharmgkbrs587783510
gwascentralrs587783510
openSNPrs587783510
23andMers587783510
23andMe allrs587783510
SNP Nexus

SNPshotrs587783510
SNPdbers587783510
MSV3drs587783510
GWAS Ctlgrs587783510
Max Magnitude0
ClinVar
Risk rs587783510(T;T)
Alt rs587783510(T;T)
Reference rs587783510(C;C)
Significance Pathogenic
Disease Rubinstein-Taybi syndrome
Variation info
Gene CREBBP
CLNDBN Rubinstein-Taybi syndrome
Reversed 1
HGVS NC_000016.9:g.3778960G>A
CLNSRC
CLNACC RCV000145775.1,