rs587783909

Orientation

plus

Stabilized

plus

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

Make rs587783909(-;-)

Make rs587783909(-;G)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

36985891

Gene

NIPBL

is a	snp
is	mentioned by
dbSNP	rs587783909
dbSNP (classic)	rs587783909
ClinGen	rs587783909
ebi	rs587783909
HLI	rs587783909
Exac	rs587783909
Gnomad	rs587783909
Varsome	rs587783909
LitVar	rs587783909
Map	rs587783909
PheGenI	rs587783909
Biobank	rs587783909
1000 genomes	rs587783909
hgdp	rs587783909
ensembl	rs587783909
geneview	rs587783909
scholar	rs587783909
google	rs587783909
pharmgkb	rs587783909
gwascentral	rs587783909
openSNP	rs587783909
23andMe	rs587783909
SNPshot	rs587783909
SNPdbe	rs587783909
MSV3d	rs587783909
GWAS Ctlg	rs587783909

Max Magnitude

0

ClinVar
Risk	rs587783909(-;-)
Alt	rs587783909(-;-)
Reference	Rs587783909(G;G)
Significance	Pathogenic
Disease	Cornelia de Lange syndrome 1
Variation	info
Gene	NIPBL
CLNDBN	Cornelia de Lange syndrome 1
Reversed	0
HGVS	NC_000005.9:g.36985993delG
CLNSRC
CLNACC	RCV000146555.1,