rs121908070

Orientation

plus

Stabilized

plus

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

Make rs121908070(C;T)

Make rs121908070(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

177238273

Gene

NSD1

is a	snp
is	mentioned by
dbSNP	rs121908070
dbSNP (classic)	rs121908070
ClinGen	rs121908070
ebi	rs121908070
HLI	rs121908070
Exac	rs121908070
Gnomad	rs121908070
Varsome	rs121908070
LitVar	rs121908070
Map	rs121908070
PheGenI	rs121908070
Biobank	rs121908070
1000 genomes	rs121908070
hgdp	rs121908070
ensembl	rs121908070
geneview	rs121908070
scholar	rs121908070
google	rs121908070
pharmgkb	rs121908070
gwascentral	rs121908070
openSNP	rs121908070
23andMe	rs121908070
SNPshot	rs121908070
SNPdbe	rs121908070
MSV3d	rs121908070
GWAS Ctlg	rs121908070

Max Magnitude

0

OMIM	606681
Desc
Variant	0010
Related	also

ClinVar
Risk	rs121908070(T;T)
Alt	rs121908070(T;T)
Reference	Rs121908070(C;C)
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.176665274C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004359.4, RCV000487238.1,