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rs879253953

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CGAG;CGAG) 0 common in clinvar
Make rs879253953(-;-)
Make rs879253953(-;CGAG)
ReferenceGRCh38.p7 38.3/149
Chromosome19
Position10154672
GeneDNMT1
is asnp
is mentioned by
dbSNPrs879253953
dbSNP (classic)rs879253953
ClinGenrs879253953
ebirs879253953
HLIrs879253953
Exacrs879253953
Gnomadrs879253953
Varsomers879253953
LitVarrs879253953
Maprs879253953
PheGenIrs879253953
Biobankrs879253953
1000 genomesrs879253953
hgdprs879253953
ensemblrs879253953
geneviewrs879253953
scholarrs879253953
googlers879253953
pharmgkbrs879253953
gwascentralrs879253953
openSNPrs879253953
23andMers879253953
SNPshotrs879253953
SNPdbers879253953
MSV3drs879253953
GWAS Ctlgrs879253953
Max Magnitude0
ClinVar
Risk rs879253953(-;-)
Alt rs879253953(-;-)
Reference Rs879253953(CGAG;CGAG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DNMT1
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.10265348_10265351delCTCG
CLNSRC
CLNACC RCV000235546.1,