rs16999593

plus

Geno	Mag	Summary
(T;T)	0	common in complete genomics

Make rs16999593(C;C)

Make rs16999593(C;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

10180505

Gene

DNMT1

is a	snp
is	mentioned by
dbSNP	rs16999593
dbSNP (classic)	rs16999593
ClinGen	rs16999593
ebi	rs16999593
HLI	rs16999593
Exac	rs16999593
Gnomad	rs16999593
Varsome	rs16999593
LitVar	rs16999593
Map	rs16999593
PheGenI	rs16999593
Biobank	rs16999593
1000 genomes	rs16999593
hgdp	rs16999593
ensembl	rs16999593
geneview	rs16999593
scholar	rs16999593
google	rs16999593
pharmgkb	rs16999593
gwascentral	rs16999593
openSNP	rs16999593
23andMe	rs16999593
SNPshot	rs16999593
SNPdbe	rs16999593
MSV3d	rs16999593
GWAS Ctlg	rs16999593

GMAF

0.05877

Max Magnitude

0

?

(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

[PMID 23049933 ] 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]

ClinVar
Risk	rs16999593(C;C)
Alt	rs16999593(C;C)
Reference	Rs16999593(T;T)
Significance	Non-pathogenic
Disease	not specified Dementia
Variation	info
Gene	DNMT1
CLNDBN	not specified Dementia, Deafness, and Sensory Neuropathy
Reversed	0
HGVS	NC_000019.9:g.10291181T>C
CLNSRC
CLNACC	RCV000246863.2, RCV000284312.1,

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