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rs1064794050

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome11
Position2135446
GeneIGF2, INS-IGF2, MIR483
is asnp
is mentioned by
dbSNPrs1064794050
dbSNP (old)rs1064794050
ClinGenrs1064794050
ebirs1064794050
HLIrs1064794050
Exacrs1064794050
Gnomadrs1064794050
Varsomers1064794050
LitVarrs1064794050
Maprs1064794050
PheGenIrs1064794050
Biobankrs1064794050
1000 genomesrs1064794050
hgdprs1064794050
ensemblrs1064794050
gopubmedrs1064794050
geneviewrs1064794050
scholarrs1064794050
googlers1064794050
pharmgkbrs1064794050
gwascentralrs1064794050
openSNPrs1064794050
23andMers1064794050
23andMe allrs1064794050
SNPshotrs1064794050
SNPdbers1064794050
MSV3drs1064794050
GWAS Ctlgrs1064794050
Max Magnitude0
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,