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rs786205234

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205234(-;-)
Make rs786205234(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2885041
GeneCDKN1C
is asnp
is mentioned by
dbSNPrs786205234
ebirs786205234
HLIrs786205234
Exacrs786205234
Varsomers786205234
Maprs786205234
PheGenIrs786205234
hapmaprs786205234
1000 genomesrs786205234
hgdprs786205234
ensemblrs786205234
gopubmedrs786205234
geneviewrs786205234
scholarrs786205234
googlers786205234
pharmgkbrs786205234
gwascentralrs786205234
openSNPrs786205234
23andMers786205234
23andMe allrs786205234
SNP Nexus

SNPshotrs786205234
SNPdbers786205234
MSV3drs786205234
GWAS Ctlgrs786205234
Max Magnitude0
ClinVar
Risk rs786205234(;)
Alt rs786205234(;)
Reference rs786205234(C;C)
Significance Pathogenic
Disease Beckwith-Wiedemann syndrome
Variation info
Gene CDKN1C
CLNDBN Beckwith-Wiedemann syndrome
Reversed 1
HGVS NC_000011.9:g.2906271delG
CLNSRC
CLNACC RCV000172982.1,