rs121908067

Orientation

plus

Stabilized

plus

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

Make rs121908067(C;G)

Make rs121908067(G;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

177209709

Gene

NSD1

is a	snp
is	mentioned by
dbSNP	rs121908067
dbSNP (classic)	rs121908067
ClinGen	rs121908067
ebi	rs121908067
HLI	rs121908067
Exac	rs121908067
Gnomad	rs121908067
Varsome	rs121908067
LitVar	rs121908067
Map	rs121908067
PheGenI	rs121908067
Biobank	rs121908067
1000 genomes	rs121908067
hgdp	rs121908067
ensembl	rs121908067
geneview	rs121908067
scholar	rs121908067
google	rs121908067
pharmgkb	rs121908067
gwascentral	rs121908067
openSNP	rs121908067
23andMe	rs121908067
SNPshot	rs121908067
SNPdbe	rs121908067
MSV3d	rs121908067
GWAS Ctlg	rs121908067

Max Magnitude

0

OMIM	606681
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121908067(G;G)
Alt	rs121908067(G;G)
Reference	Rs121908067(C;C)
Significance	Pathogenic
Disease	Sotos syndrome 1
Variation	info
Gene	NSD1
CLNDBN	Sotos syndrome 1
Reversed	0
HGVS	NC_000005.9:g.176636710C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004351.3,