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rs786205237

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205237(-;-)
Make rs786205237(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2884855
GeneCDKN1C
is asnp
is mentioned by
dbSNPrs786205237
ebirs786205237
HLIrs786205237
Exacrs786205237
Varsomers786205237
Maprs786205237
PheGenIrs786205237
hapmaprs786205237
1000 genomesrs786205237
hgdprs786205237
ensemblrs786205237
gopubmedrs786205237
geneviewrs786205237
scholarrs786205237
googlers786205237
pharmgkbrs786205237
gwascentralrs786205237
openSNPrs786205237
23andMers786205237
23andMe allrs786205237
SNP Nexus

SNPshotrs786205237
SNPdbers786205237
MSV3drs786205237
GWAS Ctlgrs786205237
Max Magnitude0
ClinVar
Risk rs786205237(;)
Alt rs786205237(;)
Reference rs786205237(C;C)
Significance Pathogenic
Disease Beckwith-Wiedemann syndrome
Variation info
Gene CDKN1C
CLNDBN Beckwith-Wiedemann syndrome
Reversed 1
HGVS NC_000011.9:g.2906085delG
CLNSRC
CLNACC RCV000172986.1,