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rs1057524802

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524802(C;C)
Make rs1057524802(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position3729724
GeneCREBBP
is asnp
is mentioned by
dbSNPrs1057524802
dbSNP (old)rs1057524802
ClinGenrs1057524802
ebirs1057524802
HLIrs1057524802
Exacrs1057524802
Gnomadrs1057524802
Varsomers1057524802
LitVarrs1057524802
Maprs1057524802
PheGenIrs1057524802
Biobankrs1057524802
1000 genomesrs1057524802
hgdprs1057524802
ensemblrs1057524802
gopubmedrs1057524802
geneviewrs1057524802
scholarrs1057524802
googlers1057524802
pharmgkbrs1057524802
gwascentralrs1057524802
openSNPrs1057524802
23andMers1057524802
23andMe allrs1057524802
SNPshotrs1057524802
SNPdbers1057524802
MSV3drs1057524802
GWAS Ctlgrs1057524802
Max Magnitude0
ClinVar
Risk rs1057524802(C;C)
Alt rs1057524802(C;C)
Reference Rs1057524802(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CREBBP
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.3779725A>G
CLNSRC
CLNACC RCV000443507.1,