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rs1057520652

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520652(C;T)
Make rs1057520652(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position3773912
GeneCREBBP
is asnp
is mentioned by
dbSNPrs1057520652
dbSNP (old)rs1057520652
ClinGenrs1057520652
ebirs1057520652
HLIrs1057520652
Exacrs1057520652
Gnomadrs1057520652
Varsomers1057520652
Maprs1057520652
PheGenIrs1057520652
Biobankrs1057520652
1000 genomesrs1057520652
hgdprs1057520652
ensemblrs1057520652
gopubmedrs1057520652
geneviewrs1057520652
scholarrs1057520652
googlers1057520652
pharmgkbrs1057520652
gwascentralrs1057520652
openSNPrs1057520652
23andMers1057520652
23andMe allrs1057520652
SNPshotrs1057520652
SNPdbers1057520652
MSV3drs1057520652
GWAS Ctlgrs1057520652
Max Magnitude0
ClinVar
Risk rs1057520652(T;T)
Alt rs1057520652(T;T)
Reference Rs1057520652(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CREBBP
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.3823913G>A
CLNSRC
CLNACC RCV000431043.1,