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rs587777507

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777507(A;G)
Make rs587777507(G;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position25241701
GeneDNMT3A
is asnp
is mentioned by
dbSNPrs587777507
ebirs587777507
HLIrs587777507
Exacrs587777507
Varsomers587777507
Maprs587777507
PheGenIrs587777507
hapmaprs587777507
1000 genomesrs587777507
hgdprs587777507
ensemblrs587777507
gopubmedrs587777507
geneviewrs587777507
scholarrs587777507
googlers587777507
pharmgkbrs587777507
gwascentralrs587777507
openSNPrs587777507
23andMers587777507
23andMe allrs587777507
SNP Nexus

SNPshotrs587777507
SNPdbers587777507
MSV3drs587777507
GWAS Ctlgrs587777507
Max Magnitude0
ClinVar
Risk rs587777507(A,G;A,G)
Alt rs587777507(A,G;A,G)
Reference rs587777507(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.25464570A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000128559.2,