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rs16999593

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs16999593(C;C)
Make rs16999593(C;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position10180505
GeneDNMT1
is asnp
is mentioned by
dbSNPrs16999593
ebirs16999593
HLIrs16999593
Exacrs16999593
Varsomers16999593
Maprs16999593
PheGenIrs16999593
hapmaprs16999593
1000 genomesrs16999593
hgdprs16999593
ensemblrs16999593
gopubmedrs16999593
geneviewrs16999593
scholarrs16999593
googlers16999593
pharmgkbrs16999593
gwascentralrs16999593
openSNPrs16999593
23andMers16999593
23andMe allrs16999593
SNP Nexus

SNPshotrs16999593
SNPdbers16999593
MSV3drs16999593
GWAS Ctlgrs16999593
GMAF0.05877
Max Magnitude0
? (C;C) (C;T) (T;T) 28

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


GET Evidence
DNMT1-H97R
aa_change His97Arg
aa_change_short H97R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.00148726
summary



[PMID 23049933OA-icon.png] Polymorphisms of the DNA methyltransferase 1 associated with reduced risks of Helicobacter pylori infection and increased risks of gastric atrophy


[PMID 23771421] Lack of association between DNMT1 gene polymorphisms and noise-induced hearing loss in a Chinese population


[PMID 24630008] [Association between SNPs in DNMT1 and noise-induced hearing loss in Chinese Han population]