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rs2228611

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2228611(A;G)
Make rs2228611(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position10156401
GeneDNMT1
is asnp
is mentioned by
dbSNPrs2228611
dbSNP (classic)rs2228611
ClinGenrs2228611
ebirs2228611
HLIrs2228611
Exacrs2228611
Gnomadrs2228611
Varsomers2228611
LitVarrs2228611
Maprs2228611
PheGenIrs2228611
Biobankrs2228611
1000 genomesrs2228611
hgdprs2228611
ensemblrs2228611
geneviewrs2228611
scholarrs2228611
googlers2228611
pharmgkbrs2228611
gwascentralrs2228611
openSNPrs2228611
23andMers2228611
SNPshotrs2228611
SNPdbers2228611
MSV3drs2228611
GWAS Ctlgrs2228611
GMAF0.4628
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 20920981] Association of DNMT1 Gene Polymorphisms in Exons With Sporadic Infiltrating Ductal Breast Carcinoma Among Chinese Han Women in the Heilongjiang Province


[PMID 22382075OA-icon.png] Low-level environmental cadmium exposure is associated with DNA hypomethylation in Argentinean women.


[PMID 23666104OA-icon.png] DNMT1, DNMT3A and DNMT3B gene variants in relation to ovarian cancer risk in the Polish population


ClinVar
Risk rs2228611(G;G)
Alt rs2228611(G;G)
Reference Rs2228611(A;A)
Significance Non-pathogenic
Disease not specified Dementia
Variation info
Gene DNMT1
CLNDBN not specified Dementia, Deafness, and Sensory Neuropathy
Reversed 1
HGVS NC_000019.9:g.10267077T>C
CLNSRC
CLNACC RCV000245855.1, RCV000385434.1,



[PMID 28323001] DNA methyltransferase 1 rs16999593 genetic polymorphism decreases risk in patients with transposition of great arteries.


[PMID 28414276] Studying the Association between Sudden Hearing Loss and DNA N-Methyltransferase 1 (DNMT1) Genetic Polymorphism.