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rs797045445

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045445(C;T)
Make rs797045445(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2884796
GeneCDKN1C
is asnp
is mentioned by
dbSNPrs797045445
ebirs797045445
HLIrs797045445
Exacrs797045445
Varsomers797045445
Maprs797045445
PheGenIrs797045445
hapmaprs797045445
1000 genomesrs797045445
hgdprs797045445
ensemblrs797045445
gopubmedrs797045445
geneviewrs797045445
scholarrs797045445
googlers797045445
pharmgkbrs797045445
gwascentralrs797045445
openSNPrs797045445
23andMers797045445
23andMe allrs797045445
SNP Nexus

SNPshotrs797045445
SNPdbers797045445
MSV3drs797045445
GWAS Ctlgrs797045445
Max Magnitude0
ClinVar
Risk rs797045445(T;T)
Alt rs797045445(T;T)
Reference rs797045445(C;C)
Significance Pathogenic
Disease Beckwith-Wiedemann syndrome
Variation info
Gene CDKN1C
CLNDBN Beckwith-Wiedemann syndrome
Reversed 1
HGVS NC_000011.9:g.2906026G>A
CLNSRC
CLNACC RCV000192927.1,