rs398124608

Orientation

plus

Stabilized

plus

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

Make rs398124608(-;-)

Make rs398124608(-;C)

Reference

GRCh38 38.1/141

Chromosome

X

Position

17376157

Gene

NHS

is a	snp
is	mentioned by
dbSNP	rs398124608
dbSNP (classic)	rs398124608
ClinGen	rs398124608
ebi	rs398124608
HLI	rs398124608
Exac	rs398124608
Gnomad	rs398124608
Varsome	rs398124608
LitVar	rs398124608
Map	rs398124608
PheGenI	rs398124608
Biobank	rs398124608
1000 genomes	rs398124608
hgdp	rs398124608
ensembl	rs398124608
geneview	rs398124608
scholar	rs398124608
google	rs398124608
pharmgkb	rs398124608
gwascentral	rs398124608
openSNP	rs398124608
23andMe	rs398124608
SNPshot	rs398124608
SNPdbe	rs398124608
MSV3d	rs398124608
GWAS Ctlg	rs398124608

Max Magnitude

0

ClinVar
Risk	rs398124608(-;-)
Alt	rs398124608(-;-)
Reference	Rs398124608(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	NHS
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.17394280delC
CLNSRC	HGMD
CLNACC	RCV000082803.4,