rs137853862

Orientation

plus

Stabilized

plus

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

Make rs137853862(A;A)

Make rs137853862(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

152858872

Gene

NSDHL

is a	snp
is	mentioned by
dbSNP	rs137853862
dbSNP (classic)	rs137853862
ClinGen	rs137853862
ebi	rs137853862
HLI	rs137853862
Exac	rs137853862
Gnomad	rs137853862
Varsome	rs137853862
LitVar	rs137853862
Map	rs137853862
PheGenI	rs137853862
Biobank	rs137853862
1000 genomes	rs137853862
hgdp	rs137853862
ensembl	rs137853862
geneview	rs137853862
scholar	rs137853862
google	rs137853862
pharmgkb	rs137853862
gwascentral	rs137853862
openSNP	rs137853862
23andMe	rs137853862
SNPshot	rs137853862
SNPdbe	rs137853862
MSV3d	rs137853862
GWAS Ctlg	rs137853862

Max Magnitude

0

ClinVar
Risk	rs137853862(A;A)
Alt	rs137853862(A;A)
Reference	Rs137853862(G;G)
Significance	Pathogenic
Disease	Child syndrome
Variation	info
Gene	NSDHL
CLNDBN	Child syndrome
Reversed	0
HGVS	NC_000023.10:g.152027416G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000020429.1,

OMIM	308050
Desc
Variant
Related	also