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rs144689354

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs144689354(A;A)
Make rs144689354(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position25243931
GeneDNMT3A
is asnp
is mentioned by
dbSNPrs144689354
dbSNP (old)rs144689354
ClinGenrs144689354
ebirs144689354
HLIrs144689354
Exacrs144689354
Gnomadrs144689354
Varsomers144689354
LitVarrs144689354
Maprs144689354
PheGenIrs144689354
Biobankrs144689354
1000 genomesrs144689354
hgdprs144689354
ensemblrs144689354
gopubmedrs144689354
geneviewrs144689354
scholarrs144689354
googlers144689354
pharmgkbrs144689354
gwascentralrs144689354
openSNPrs144689354
23andMers144689354
23andMe allrs144689354
SNPshotrs144689354
SNPdbers144689354
MSV3drs144689354
GWAS Ctlgrs144689354
Max Magnitude0
ClinVar
Risk rs144689354(A;A)
Alt rs144689354(A;A)
Reference Rs144689354(G;G)
Significance Probable-Pathogenic
Disease Tatton-Brown-rahman syndrome not provided
Variation info
Gene DNMT3A
CLNDBN Tatton-Brown-rahman syndrome not provided
Reversed 0
HGVS NC_000002.11:g.25466800G>A
CLNSRC
CLNACC RCV000367312.1, RCV000433567.1,