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

rs137852766

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852766(C;T)
Make rs137852766(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2885351
GeneCDKN1C
is asnp
is mentioned by
dbSNPrs137852766
ebirs137852766
HLIrs137852766
Exacrs137852766
Varsomers137852766
Maprs137852766
PheGenIrs137852766
hapmaprs137852766
1000 genomesrs137852766
hgdprs137852766
ensemblrs137852766
gopubmedrs137852766
geneviewrs137852766
scholarrs137852766
googlers137852766
pharmgkbrs137852766
gwascentralrs137852766
openSNPrs137852766
23andMers137852766
23andMe allrs137852766
SNP Nexus

SNPshotrs137852766
SNPdbers137852766
MSV3drs137852766
GWAS Ctlgrs137852766
Max Magnitude0
OMIM600856
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137852766(T;T)
Alt rs137852766(T;T)
Reference rs137852766(C;C)
Significance Pathogenic
Disease Beckwith-Wiedemann syndrome
Variation info
Gene CDKN1C
CLNDBN Beckwith-Wiedemann syndrome
Reversed 1
HGVS NC_000011.9:g.2906581G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009287.2,