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

rs797044860

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044860(A;G)
Make rs797044860(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position3736801
GeneCREBBP
is asnp
is mentioned by
dbSNPrs797044860
ebirs797044860
HLIrs797044860
Exacrs797044860
Varsomers797044860
Maprs797044860
PheGenIrs797044860
hapmaprs797044860
1000 genomesrs797044860
hgdprs797044860
ensemblrs797044860
gopubmedrs797044860
geneviewrs797044860
scholarrs797044860
googlers797044860
pharmgkbrs797044860
gwascentralrs797044860
openSNPrs797044860
23andMers797044860
23andMe allrs797044860
SNP Nexus

SNPshotrs797044860
SNPdbers797044860
MSV3drs797044860
GWAS Ctlgrs797044860
Max Magnitude0
ClinVar
Risk rs797044860(G;G)
Alt rs797044860(G;G)
Reference rs797044860(A;A)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene CREBBP
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000016.9:g.3786802T>C
CLNSRC
CLNACC RCV000190664.1,