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rs1057518115

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518115(C;C)
Make rs1057518115(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position2135427
GeneIGF2, INS-IGF2, MIR483
is asnp
is mentioned by
dbSNPrs1057518115
dbSNP (old)rs1057518115
ClinGenrs1057518115
ebirs1057518115
HLIrs1057518115
Exacrs1057518115
Gnomadrs1057518115
Varsomers1057518115
LitVarrs1057518115
Maprs1057518115
PheGenIrs1057518115
Biobankrs1057518115
1000 genomesrs1057518115
hgdprs1057518115
ensemblrs1057518115
gopubmedrs1057518115
geneviewrs1057518115
scholarrs1057518115
googlers1057518115
pharmgkbrs1057518115
gwascentralrs1057518115
openSNPrs1057518115
23andMers1057518115
23andMe allrs1057518115
SNPshotrs1057518115
SNPdbers1057518115
MSV3drs1057518115
GWAS Ctlgrs1057518115
Max Magnitude0
ClinVar
Risk rs1057518115(C;C)
Alt rs1057518115(C;C)
Reference Rs1057518115(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIR483 IGF2 INS-IGF2
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.2156657A>G
CLNSRC
CLNACC RCV000414320.1,