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rs786205235

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs786205235(-;C)
Make rs786205235(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2885156
GeneCDKN1C
is asnp
is mentioned by
dbSNPrs786205235
ClinGenrs786205235
ebirs786205235
HLIrs786205235
Exacrs786205235
Varsomers786205235
Maprs786205235
PheGenIrs786205235
hapmaprs786205235
1000 genomesrs786205235
hgdprs786205235
ensemblrs786205235
gopubmedrs786205235
geneviewrs786205235
scholarrs786205235
googlers786205235
pharmgkbrs786205235
gwascentralrs786205235
openSNPrs786205235
23andMers786205235
23andMe allrs786205235
SNP Nexus

SNPshotrs786205235
SNPdbers786205235
MSV3drs786205235
GWAS Ctlgrs786205235
Max Magnitude0
ClinVar
Risk rs786205235(C;C)
Alt rs786205235(C;C)
Reference Rs786205235(-;-)
Significance Pathogenic
Disease Beckwith-Wiedemann syndrome
Variation info
Gene CDKN1C
CLNDBN Beckwith-Wiedemann syndrome
Reversed 1
HGVS NC_000011.9:g.2906387dupG
CLNSRC
CLNACC RCV000172989.1,