rs144689354

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs144689354(A;A)

Make rs144689354(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

2

Position

25243931

Gene

DNMT3A

is a	snp
is	mentioned by
dbSNP	rs144689354
dbSNP (classic)	rs144689354
ClinGen	rs144689354
ebi	rs144689354
HLI	rs144689354
Exac	rs144689354
Gnomad	rs144689354
Varsome	rs144689354
LitVar	rs144689354
Map	rs144689354
PheGenI	rs144689354
Biobank	rs144689354
1000 genomes	rs144689354
hgdp	rs144689354
ensembl	rs144689354
geneview	rs144689354
scholar	rs144689354
google	rs144689354
pharmgkb	rs144689354
gwascentral	rs144689354
openSNP	rs144689354
23andMe	rs144689354
SNPshot	rs144689354
SNPdbe	rs144689354
MSV3d	rs144689354
GWAS Ctlg	rs144689354

Max Magnitude

0

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,