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rs10732516

From SNPedia

Orientationplus
Stabilizedplus
Make rs10732516(A;A)
Make rs10732516(A;G)
Make rs10732516(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position1999976
is asnp
is mentioned by
dbSNPrs10732516
ebirs10732516
HLIrs10732516
Exacrs10732516
Varsomers10732516
Maprs10732516
PheGenIrs10732516
hapmaprs10732516
1000 genomesrs10732516
hgdprs10732516
ensemblrs10732516
gopubmedrs10732516
geneviewrs10732516
scholarrs10732516
googlers10732516
pharmgkbrs10732516
gwascentralrs10732516
openSNPrs10732516
23andMers10732516
23andMe allrs10732516
SNP Nexus

SNPshotrs10732516
SNPdbers10732516
MSV3drs10732516
GWAS Ctlgrs10732516
GMAF0.3476
Max Magnitude

[PMID 21991322OA-icon.png] Impact of the genome on the epigenome is manifested in DNA methylation patterns of imprinted regions in monozygotic and dizygotic twins[PMID 16839189OA-icon.png] Human imprinted chromosomal regions are historical hot-spots of recombination.

[PMID 17012269OA-icon.png] Non-random, individual-specific methylation profiles are present at the sixth CTCF binding site in the human H19/IGF2 imprinting control region.

[PMID 19936258OA-icon.png] Epigenetic features of human mesenchymal stem cells determine their permissiveness for induction of relevant transcriptional changes by SYT-SSX1.

[PMID 24575294OA-icon.png] Interplay between polymorphisms and methylation in the H19/IGF2 gene region may contribute to obesity in Mexican-American children [PMID 23725790] GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.