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rs786205495

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205495(C;C)
Make rs786205495(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position3731774
GeneCREBBP
is asnp
is mentioned by
dbSNPrs786205495
ebirs786205495
HLIrs786205495
Exacrs786205495
Varsomers786205495
Maprs786205495
PheGenIrs786205495
hapmaprs786205495
1000 genomesrs786205495
hgdprs786205495
ensemblrs786205495
gopubmedrs786205495
geneviewrs786205495
scholarrs786205495
googlers786205495
pharmgkbrs786205495
gwascentralrs786205495
openSNPrs786205495
23andMers786205495
23andMe allrs786205495
SNP Nexus

SNPshotrs786205495
SNPdbers786205495
MSV3drs786205495
GWAS Ctlgrs786205495
Max Magnitude0
ClinVar
Risk rs786205495(C;C)
Alt rs786205495(C;C)
Reference rs786205495(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CREBBP
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.3781775A>G
CLNSRC
CLNACC RCV000171243.1,