rs587784226

Orientation

plus

Stabilized

plus

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

Make rs587784226(A;A)

Make rs587784226(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

152868900

Gene

NSDHL

is a	snp
is	mentioned by
dbSNP	rs587784226
dbSNP (classic)	rs587784226
ClinGen	rs587784226
ebi	rs587784226
HLI	rs587784226
Exac	rs587784226
Gnomad	rs587784226
Varsome	rs587784226
LitVar	rs587784226
Map	rs587784226
PheGenI	rs587784226
Biobank	rs587784226
1000 genomes	rs587784226
hgdp	rs587784226
ensembl	rs587784226
geneview	rs587784226
scholar	rs587784226
google	rs587784226
pharmgkb	rs587784226
gwascentral	rs587784226
openSNP	rs587784226
23andMe	rs587784226
SNPshot	rs587784226
SNPdbe	rs587784226
MSV3d	rs587784226
GWAS Ctlg	rs587784226

Max Magnitude

0

ClinVar
Risk	rs587784226(A;A)
Alt	rs587784226(A;A)
Reference	Rs587784226(C;C)
Significance	Pathogenic
Disease	Child syndrome
Variation	info
Gene	NSDHL
CLNDBN	Child syndrome
Reversed	0
HGVS	NC_000023.10:g.152037444C>A
CLNSRC
CLNACC	RCV000146968.1,