rs587784225

Orientation

plus

Stabilized

plus

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

Make rs587784225(-;-)

Make rs587784225(-;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

152868898

Gene

NSDHL

is a	snp
is	mentioned by
dbSNP	rs587784225
dbSNP (classic)	rs587784225
ClinGen	rs587784225
ebi	rs587784225
HLI	rs587784225
Exac	rs587784225
Gnomad	rs587784225
Varsome	rs587784225
LitVar	rs587784225
Map	rs587784225
PheGenI	rs587784225
Biobank	rs587784225
1000 genomes	rs587784225
hgdp	rs587784225
ensembl	rs587784225
geneview	rs587784225
scholar	rs587784225
google	rs587784225
pharmgkb	rs587784225
gwascentral	rs587784225
openSNP	rs587784225
23andMe	rs587784225
SNPshot	rs587784225
SNPdbe	rs587784225
MSV3d	rs587784225
GWAS Ctlg	rs587784225

Max Magnitude

0

ClinVar
Risk	rs587784225(-;-)
Alt	rs587784225(-;-)
Reference	Rs587784225(T;T)
Significance	Pathogenic
Disease	Child syndrome
Variation	info
Gene	NSDHL
CLNDBN	Child syndrome
Reversed	0
HGVS	NC_000023.10:g.152037442delT
CLNSRC
CLNACC	RCV000146967.1,