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rs7354779

From SNPedia

Orientationplus
Stabilizedplus
Make rs7354779(C;C)
Make rs7354779(C;T)
Make rs7354779(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position44250887
GeneDNMT3L
is asnp
is mentioned by
dbSNPrs7354779
ebirs7354779
HLIrs7354779
Exacrs7354779
Varsomers7354779
Maprs7354779
PheGenIrs7354779
hapmaprs7354779
1000 genomesrs7354779
hgdprs7354779
ensemblrs7354779
gopubmedrs7354779
geneviewrs7354779
scholarrs7354779
googlers7354779
pharmgkbrs7354779
gwascentralrs7354779
openSNPrs7354779
23andMers7354779
23andMe allrs7354779
SNP Nexus

SNPshotrs7354779
SNPdbers7354779
MSV3drs7354779
GWAS Ctlgrs7354779
GMAF0.1804
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20593030OA-icon.png] Human intelligence and polymorphisms in the DNA methyltransferase genes involved in epigenetic marking


[PMID 22116073] Association between single-nucleotide polymorphisms of DNMT3L and infertility with azoospermia in Chinese men


[PMID 22401780] Genetic polymorphisms of DNMT3L involved in hypermethylation of chromosomal ends are associated with greater risk of developing ovarian endometriosis.


GET Evidence
DNMT3L-R278G
aa_change Arg278Gly
aa_change_short R278G
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.249303
summary



[PMID 23922667OA-icon.png] DNA methyltransferase candidate polymorphisms, imprinting methylation, and birth outcome


[PMID 26647998] Association between DNMT3L polymorphic variants and the risk of endometriosis-associated infertility.