rs766858016

Orientation

plus

Stabilized

plus

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

Make rs766858016(G;G)

Make rs766858016(G;T)

Reference

GRCh38.p7 38.3/149

Chromosome

2

Position

25247710

Gene

DNMT3A

is a	snp
is	mentioned by
dbSNP	rs766858016
dbSNP (classic)	rs766858016
ClinGen	rs766858016
ebi	rs766858016
HLI	rs766858016
Exac	rs766858016
Gnomad	rs766858016
Varsome	rs766858016
LitVar	rs766858016
Map	rs766858016
PheGenI	rs766858016
Biobank	rs766858016
1000 genomes	rs766858016
hgdp	rs766858016
ensembl	rs766858016
geneview	rs766858016
scholar	rs766858016
google	rs766858016
pharmgkb	rs766858016
gwascentral	rs766858016
openSNP	rs766858016
23andMe	rs766858016
SNPshot	rs766858016
SNPdbe	rs766858016
MSV3d	rs766858016
GWAS Ctlg	rs766858016

Max Magnitude

0

ClinVar
Risk	rs766858016(A;A) rs766858016(G;G)
Alt	rs766858016(A;A) rs766858016(G;G)
Reference	Rs766858016(T;T)
Significance	Probable-Pathogenic
Disease	Tatton-Brown-rahman syndrome
Variation	info
Gene	DNMT3A
CLNDBN	Tatton-Brown-rahman syndrome
Reversed	0
HGVS	NC_000002.11:g.25470579T>G
CLNSRC
CLNACC	RCV000256441.1,