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rs1057520589

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520589(C;T)
Make rs1057520589(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position3770791
GeneCREBBP
is asnp
is mentioned by
dbSNPrs1057520589
dbSNP (classic)rs1057520589
ClinGenrs1057520589
ebirs1057520589
HLIrs1057520589
Exacrs1057520589
Gnomadrs1057520589
Varsomers1057520589
LitVarrs1057520589
Maprs1057520589
PheGenIrs1057520589
Biobankrs1057520589
1000 genomesrs1057520589
hgdprs1057520589
ensemblrs1057520589
geneviewrs1057520589
scholarrs1057520589
googlers1057520589
pharmgkbrs1057520589
gwascentralrs1057520589
openSNPrs1057520589
23andMers1057520589
23andMe allrs1057520589
SNPshotrs1057520589
SNPdbers1057520589
MSV3drs1057520589
GWAS Ctlgrs1057520589
Max Magnitude0
ClinVar
Risk rs1057520589(T;T)
Alt rs1057520589(T;T)
Reference Rs1057520589(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CREBBP
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.3820792G>A
CLNSRC
CLNACC RCV000434050.1,