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rs786205236

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs786205236(-;G)
Make rs786205236(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2885089
GeneCDKN1C
is asnp
is mentioned by
dbSNPrs786205236
ClinGenrs786205236
ebirs786205236
HLIrs786205236
Exacrs786205236
Varsomers786205236
Maprs786205236
PheGenIrs786205236
hapmaprs786205236
1000 genomesrs786205236
hgdprs786205236
ensemblrs786205236
gopubmedrs786205236
geneviewrs786205236
scholarrs786205236
googlers786205236
pharmgkbrs786205236
gwascentralrs786205236
openSNPrs786205236
23andMers786205236
23andMe allrs786205236
SNP Nexus

SNPshotrs786205236
SNPdbers786205236
MSV3drs786205236
GWAS Ctlgrs786205236
Max Magnitude0
ClinVar
Risk rs786205236(G;G)
Alt rs786205236(G;G)
Reference Rs786205236(-;-)
Significance Pathogenic
Disease Beckwith-Wiedemann syndrome
Variation info
Gene CDKN1C
CLNDBN Beckwith-Wiedemann syndrome
Reversed 1
HGVS NC_000011.9:g.2906320dupC
CLNSRC
CLNACC RCV000172990.1,