rs587784076

Orientation

plus

Stabilized

plus

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

Make rs587784076(C;T)

Make rs587784076(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

177210209

Gene

NSD1

is a	snp
is	mentioned by
dbSNP	rs587784076
dbSNP (classic)	rs587784076
ClinGen	rs587784076
ebi	rs587784076
HLI	rs587784076
Exac	rs587784076
Gnomad	rs587784076
Varsome	rs587784076
LitVar	rs587784076
Map	rs587784076
PheGenI	rs587784076
Biobank	rs587784076
1000 genomes	rs587784076
hgdp	rs587784076
ensembl	rs587784076
geneview	rs587784076
scholar	rs587784076
google	rs587784076
pharmgkb	rs587784076
gwascentral	rs587784076
openSNP	rs587784076
23andMe	rs587784076
SNPshot	rs587784076
SNPdbe	rs587784076
MSV3d	rs587784076
GWAS Ctlg	rs587784076

Max Magnitude

0

ClinVar
Risk	rs587784076(T;T)
Alt	rs587784076(T;T)
Reference	Rs587784076(C;C)
Significance	Pathogenic
Disease	Sotos syndrome 1 not provided Beckwith-Wiedemann syndrome
Variation	info
Gene	NSD1
CLNDBN	Sotos syndrome 1 not provided Beckwith-Wiedemann syndrome
Reversed	0
HGVS	NC_000005.9:g.176637210C>T
CLNSRC
CLNACC	RCV000146770.1, RCV000431725.1, RCV000458210.1,