rs587784092

Orientation

plus

Stabilized

plus

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

Make rs587784092(-;-)

Make rs587784092(-;CT)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

177211353

Gene

NSD1

is a	snp
is	mentioned by
dbSNP	rs587784092
dbSNP (classic)	rs587784092
ClinGen	rs587784092
ebi	rs587784092
HLI	rs587784092
Exac	rs587784092
Gnomad	rs587784092
Varsome	rs587784092
LitVar	rs587784092
Map	rs587784092
PheGenI	rs587784092
Biobank	rs587784092
1000 genomes	rs587784092
hgdp	rs587784092
ensembl	rs587784092
geneview	rs587784092
scholar	rs587784092
google	rs587784092
pharmgkb	rs587784092
gwascentral	rs587784092
openSNP	rs587784092
23andMe	rs587784092
SNPshot	rs587784092
SNPdbe	rs587784092
MSV3d	rs587784092
GWAS Ctlg	rs587784092

Max Magnitude

0

ClinVar
Risk	rs587784092(-;-)
Alt	rs587784092(-;-)
Reference	Rs587784092(CT;CT)
Significance	Pathogenic
Disease	Sotos syndrome 1 not provided
Variation	info
Gene	NSD1
CLNDBN	Sotos syndrome 1 not provided
Reversed	0
HGVS	NC_000005.9:g.176638354_176638355delCT
CLNSRC
CLNACC	RCV000146796.1, RCV000330545.1,