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rs10770125

From SNPedia

Orientationplus
Stabilizedplus
Make rs10770125(A;A)
Make rs10770125(A;G)
Make rs10770125(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2147784
GeneIGF2, INS-IGF2
is asnp
is mentioned by
dbSNPrs10770125
ebirs10770125
HLIrs10770125
Exacrs10770125
Varsomers10770125
Maprs10770125
PheGenIrs10770125
hapmaprs10770125
1000 genomesrs10770125
hgdprs10770125
ensemblrs10770125
gopubmedrs10770125
geneviewrs10770125
scholarrs10770125
googlers10770125
pharmgkbrs10770125
gwascentralrs10770125
openSNPrs10770125
23andMers10770125
23andMe allrs10770125
SNP Nexus

SNPshotrs10770125
SNPdbers10770125
MSV3drs10770125
GWAS Ctlgrs10770125
GMAF0.3848
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 21926269OA-icon.png] Associations between paternally transmitted fetal IGF2 variants and maternal circulating glucose concentrations in pregnancy


[PMID 18769151OA-icon.png] A sensitive functional assay reveals frequent loss of genomic imprinting in human placenta.


GET Evidence
NM_001042376-L144P
aa_change Leu144Pro
aa_change_short L144P
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.345476
summary