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rs587777510

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777510(A;G)
Make rs587777510(G;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position25234313
GeneDNMT3A
is asnp
is mentioned by
dbSNPrs587777510
ebirs587777510
HLIrs587777510
Exacrs587777510
Varsomers587777510
Maprs587777510
PheGenIrs587777510
hapmaprs587777510
1000 genomesrs587777510
hgdprs587777510
ensemblrs587777510
gopubmedrs587777510
geneviewrs587777510
scholarrs587777510
googlers587777510
pharmgkbrs587777510
gwascentralrs587777510
openSNPrs587777510
23andMers587777510
23andMe allrs587777510
SNP Nexus

SNPshotrs587777510
SNPdbers587777510
MSV3drs587777510
GWAS Ctlgrs587777510
Max Magnitude0
ClinVar
Risk rs587777510(A,G;A,G)
Alt rs587777510(A,G;A,G)
Reference rs587777510(T;T)
Significance Pathogenic
Disease Tatton-Brown-rahman syndrome
Variation info
Gene DNMT3A
CLNDBN Tatton-Brown-rahman syndrome
Reversed 1
HGVS NC_000002.11:g.25457182A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000128562.2,