rs786205576

Orientation

plus

Stabilized

plus

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

Make rs786205576(A;A)

Make rs786205576(A;T)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

177210457

Gene

NSD1

is a	snp
is	mentioned by
dbSNP	rs786205576
dbSNP (classic)	rs786205576
ClinGen	rs786205576
ebi	rs786205576
HLI	rs786205576
Exac	rs786205576
Gnomad	rs786205576
Varsome	rs786205576
LitVar	rs786205576
Map	rs786205576
PheGenI	rs786205576
Biobank	rs786205576
1000 genomes	rs786205576
hgdp	rs786205576
ensembl	rs786205576
geneview	rs786205576
scholar	rs786205576
google	rs786205576
pharmgkb	rs786205576
gwascentral	rs786205576
openSNP	rs786205576
23andMe	rs786205576
SNPshot	rs786205576
SNPdbe	rs786205576
MSV3d	rs786205576
GWAS Ctlg	rs786205576

Max Magnitude

0

ClinVar
Risk	rs786205576(A;A)
Alt	rs786205576(A;A)
Reference	Rs786205576(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NSD1
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.176637458T>A
CLNSRC
CLNACC	RCV000171389.1,