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rs2276248

From SNPedia

Orientationplus
Stabilizedplus
Make rs2276248(C;C)
Make rs2276248(C;T)
Make rs2276248(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position44259375
GeneDNMT3L
is asnp
is mentioned by
dbSNPrs2276248
ebirs2276248
HLIrs2276248
Exacrs2276248
Varsomers2276248
Maprs2276248
PheGenIrs2276248
hapmaprs2276248
1000 genomesrs2276248
hgdprs2276248
ensemblrs2276248
gopubmedrs2276248
geneviewrs2276248
scholarrs2276248
googlers2276248
pharmgkbrs2276248
gwascentralrs2276248
openSNPrs2276248
23andMers2276248
23andMe allrs2276248
SNP Nexus

SNPshotrs2276248
SNPdbers2276248
MSV3drs2276248
GWAS Ctlgrs2276248
GMAF0.1281
Max Magnitude
? (C;C) (C;T) (T;T) 28

[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.


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