rs587784223

Orientation

plus

Stabilized

plus

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

Make rs587784223(C;T)

Make rs587784223(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

152865870

Gene

NSDHL

is a	snp
is	mentioned by
dbSNP	rs587784223
dbSNP (classic)	rs587784223
ClinGen	rs587784223
ebi	rs587784223
HLI	rs587784223
Exac	rs587784223
Gnomad	rs587784223
Varsome	rs587784223
LitVar	rs587784223
Map	rs587784223
PheGenI	rs587784223
Biobank	rs587784223
1000 genomes	rs587784223
hgdp	rs587784223
ensembl	rs587784223
geneview	rs587784223
scholar	rs587784223
google	rs587784223
pharmgkb	rs587784223
gwascentral	rs587784223
openSNP	rs587784223
23andMe	rs587784223
SNPshot	rs587784223
SNPdbe	rs587784223
MSV3d	rs587784223
GWAS Ctlg	rs587784223

Max Magnitude

0

ClinVar
Risk	rs587784223(T;T)
Alt	rs587784223(T;T)
Reference	Rs587784223(C;C)
Significance	Probable-Pathogenic
Disease	Child syndrome not specified
Variation	info
Gene	NSDHL
CLNDBN	Child syndrome not specified
Reversed	0
HGVS	NC_000023.10:g.152034414C>T
CLNSRC
CLNACC	RCV000146963.1, RCV000179494.1,