rs137853863

Orientation

plus

Stabilized

plus

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

Make rs137853863(A;G)

Make rs137853863(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

152869040

Gene

NSDHL

is a	snp
is	mentioned by
dbSNP	rs137853863
dbSNP (classic)	rs137853863
ClinGen	rs137853863
ebi	rs137853863
HLI	rs137853863
Exac	rs137853863
Gnomad	rs137853863
Varsome	rs137853863
LitVar	rs137853863
Map	rs137853863
PheGenI	rs137853863
Biobank	rs137853863
1000 genomes	rs137853863
hgdp	rs137853863
ensembl	rs137853863
geneview	rs137853863
scholar	rs137853863
google	rs137853863
pharmgkb	rs137853863
gwascentral	rs137853863
openSNP	rs137853863
23andMe	rs137853863
SNPshot	rs137853863
SNPdbe	rs137853863
MSV3d	rs137853863
GWAS Ctlg	rs137853863

Max Magnitude

0

ClinVar
Risk	rs137853863(C;C) rs137853863(G;G)
Alt	rs137853863(C;C) rs137853863(G;G)
Reference	Rs137853863(A;A)
Significance	Pathogenic
Disease	Child syndrome
Variation	info
Gene	NSDHL
CLNDBN	Child syndrome
Reversed	0
HGVS	NC_000023.10:g.152037584A>G
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020427.1,

OMIM	308050
Desc
Variant
Related	also