rs587784224

Orientation

plus

Stabilized

plus

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

Make rs587784224(A;A)

Make rs587784224(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

152867611

Gene

NSDHL

is a	snp
is	mentioned by
dbSNP	rs587784224
dbSNP (classic)	rs587784224
ClinGen	rs587784224
ebi	rs587784224
HLI	rs587784224
Exac	rs587784224
Gnomad	rs587784224
Varsome	rs587784224
LitVar	rs587784224
Map	rs587784224
PheGenI	rs587784224
Biobank	rs587784224
1000 genomes	rs587784224
hgdp	rs587784224
ensembl	rs587784224
geneview	rs587784224
scholar	rs587784224
google	rs587784224
pharmgkb	rs587784224
gwascentral	rs587784224
openSNP	rs587784224
23andMe	rs587784224
SNPshot	rs587784224
SNPdbe	rs587784224
MSV3d	rs587784224
GWAS Ctlg	rs587784224

Max Magnitude

0

ClinVar
Risk	rs587784224(A;A)
Alt	rs587784224(A;A)
Reference	Rs587784224(G;G)
Significance	Probable-Pathogenic
Disease	Child syndrome not specified not provided
Variation	info
Gene	NSDHL
CLNDBN	Child syndrome not specified not provided
Reversed	0
HGVS	NC_000023.10:g.152036155G>A
CLNSRC
CLNACC	RCV000146964.1, RCV000374267.1, RCV000412977.1,