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rs16999358

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs16999358(A;A)
Make rs16999358(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position10162679
GeneDNMT1
is asnp
is mentioned by
dbSNPrs16999358
dbSNP (old)rs16999358
ClinGenrs16999358
ebirs16999358
HLIrs16999358
Exacrs16999358
Gnomadrs16999358
Varsomers16999358
Maprs16999358
PheGenIrs16999358
Biobankrs16999358
1000 genomesrs16999358
hgdprs16999358
ensemblrs16999358
gopubmedrs16999358
geneviewrs16999358
scholarrs16999358
googlers16999358
pharmgkbrs16999358
gwascentralrs16999358
openSNPrs16999358
23andMers16999358
23andMe allrs16999358
SNPshotrs16999358
SNPdbers16999358
MSV3drs16999358
GWAS Ctlgrs16999358
Max Magnitude0
? (A;A) (A;G) (G;G) 28

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

ClinVar
Risk rs16999358(A;A)
Alt rs16999358(A;A)
Reference Rs16999358(G;G)
Significance Non-pathogenic
Disease Dementia
Variation info
Gene DNMT1
CLNDBN Dementia, Deafness, and Sensory Neuropathy
Reversed 0
HGVS NC_000019.9:g.10273355G>A
CLNSRC
CLNACC RCV000379095.1,