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rs587777866

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777866(C;C)
Make rs587777866(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2883997
GeneCDKN1C
is asnp
is mentioned by
dbSNPrs587777866
ebirs587777866
HLIrs587777866
Exacrs587777866
Varsomers587777866
Maprs587777866
PheGenIrs587777866
hapmaprs587777866
1000 genomesrs587777866
hgdprs587777866
ensemblrs587777866
gopubmedrs587777866
geneviewrs587777866
scholarrs587777866
googlers587777866
pharmgkbrs587777866
gwascentralrs587777866
openSNPrs587777866
23andMers587777866
23andMe allrs587777866
SNP Nexus

SNPshotrs587777866
SNPdbers587777866
MSV3drs587777866
GWAS Ctlgrs587777866
Max Magnitude0
ClinVar
Risk rs587777866(C;C)
Alt rs587777866(C;C)
Reference rs587777866(T;T)
Significance Pathogenic
Disease Beckwith-Wiedemann syndrome
Variation info
Gene CDKN1C
CLNDBN Beckwith-Wiedemann syndrome
Reversed 1
HGVS NC_000011.9:g.2905227A>G
CLNSRC
CLNACC RCV000172924.1,