rs786205237

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs786205237(-;-)

Make rs786205237(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

2884855

Gene	CDKN1C, LOC107987413

is a	snp
is	mentioned by
dbSNP	rs786205237
dbSNP (classic)	rs786205237
ClinGen	rs786205237
ebi	rs786205237
HLI	rs786205237
Exac	rs786205237
Gnomad	rs786205237
Varsome	rs786205237
LitVar	rs786205237
Map	rs786205237
PheGenI	rs786205237
Biobank	rs786205237
1000 genomes	rs786205237
hgdp	rs786205237
ensembl	rs786205237
geneview	rs786205237
scholar	rs786205237
google	rs786205237
pharmgkb	rs786205237
gwascentral	rs786205237
openSNP	rs786205237
23andMe	rs786205237
SNPshot	rs786205237
SNPdbe	rs786205237
MSV3d	rs786205237
GWAS Ctlg	rs786205237

Max Magnitude

0

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,