rs587777507

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(T;T)	0	common in clinvar

Make rs587777507(A;G)

Make rs587777507(G;G)

Reference

GRCh38 38.1/142

Chromosome

2

Position

25241701

Gene

DNMT3A

is a	snp
is	mentioned by
dbSNP	rs587777507
dbSNP (classic)	rs587777507
ClinGen	rs587777507
ebi	rs587777507
HLI	rs587777507
Exac	rs587777507
Gnomad	rs587777507
Varsome	rs587777507
LitVar	rs587777507
Map	rs587777507
PheGenI	rs587777507
Biobank	rs587777507
1000 genomes	rs587777507
hgdp	rs587777507
ensembl	rs587777507
geneview	rs587777507
scholar	rs587777507
google	rs587777507
pharmgkb	rs587777507
gwascentral	rs587777507
openSNP	rs587777507
23andMe	rs587777507
SNPshot	rs587777507
SNPdbe	rs587777507
MSV3d	rs587777507
GWAS Ctlg	rs587777507

Max Magnitude

0

ClinVar
Risk	Rs587777507(A;A) rs587777507(G;G)
Alt	Rs587777507(A;A) rs587777507(G;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 UniProtKB (protein)
CLNACC	RCV000128559.2,