rs1064794050

Orientation

minus

Stabilized

minus

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

Chromosome

11

Position

2135446

Gene	IGF2, INS-IGF2, MIR483

is a	snp
is	mentioned by
dbSNP	rs1064794050
dbSNP (classic)	rs1064794050
ClinGen	rs1064794050
ebi	rs1064794050
HLI	rs1064794050
Exac	rs1064794050
Gnomad	rs1064794050
Varsome	rs1064794050
LitVar	rs1064794050
Map	rs1064794050
PheGenI	rs1064794050
Biobank	rs1064794050
1000 genomes	rs1064794050
hgdp	rs1064794050
ensembl	rs1064794050
geneview	rs1064794050
scholar	rs1064794050
google	rs1064794050
pharmgkb	rs1064794050
gwascentral	rs1064794050
openSNP	rs1064794050
23andMe	rs1064794050
SNPshot	rs1064794050
SNPdbe	rs1064794050
MSV3d	rs1064794050
GWAS Ctlg	rs1064794050

Max Magnitude

0

ClinVar
Risk	rs1064794050(G;G)
Alt	rs1064794050(G;G)
Reference	Rs1064794050(C;C)
Significance	Pathogenic
Disease	not provided Russell-Silver syndrome
Variation	info
Gene	MIR483 IGF2 INS-IGF2
CLNDBN	not provided Russell-Silver syndrome
Reversed	1
HGVS	NC_000011.9:g.2156676G>C
CLNSRC
CLNACC	RCV000479354.1, RCV000491853.1,