Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518498

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518498(G;T)
Make rs1057518498(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position3793502
GeneCREBBP
is asnp
is mentioned by
dbSNPrs1057518498
dbSNP (classic)rs1057518498
ClinGenrs1057518498
ebirs1057518498
HLIrs1057518498
Exacrs1057518498
Gnomadrs1057518498
Varsomers1057518498
LitVarrs1057518498
Maprs1057518498
PheGenIrs1057518498
Biobankrs1057518498
1000 genomesrs1057518498
hgdprs1057518498
ensemblrs1057518498
geneviewrs1057518498
scholarrs1057518498
googlers1057518498
pharmgkbrs1057518498
gwascentralrs1057518498
openSNPrs1057518498
23andMers1057518498
SNPshotrs1057518498
SNPdbers1057518498
MSV3drs1057518498
GWAS Ctlgrs1057518498
Max Magnitude0
ClinVar
Risk rs1057518498(T;T)
Alt rs1057518498(T;T)
Reference Rs1057518498(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CREBBP
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.3843503C>A
CLNSRC
CLNACC RCV000414631.1,