rs587783898

Orientation

plus

Stabilized

plus

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

Make rs587783898(-;-)

Make rs587783898(-;C)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

36985288

Gene

NIPBL

is a	snp
is	mentioned by
dbSNP	rs587783898
dbSNP (classic)	rs587783898
ClinGen	rs587783898
ebi	rs587783898
HLI	rs587783898
Exac	rs587783898
Gnomad	rs587783898
Varsome	rs587783898
LitVar	rs587783898
Map	rs587783898
PheGenI	rs587783898
Biobank	rs587783898
1000 genomes	rs587783898
hgdp	rs587783898
ensembl	rs587783898
geneview	rs587783898
scholar	rs587783898
google	rs587783898
pharmgkb	rs587783898
gwascentral	rs587783898
openSNP	rs587783898
23andMe	rs587783898
SNPshot	rs587783898
SNPdbe	rs587783898
MSV3d	rs587783898
GWAS Ctlg	rs587783898

Max Magnitude

0

ClinVar
Risk	rs587783898(-;-)
Alt	rs587783898(-;-)
Reference	Rs587783898(C;C)
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.36985390delC
CLNSRC
CLNACC	RCV000146537.1,