rs864309679

Orientation

plus

Stabilized

plus

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

Make rs864309679(-;-)

Make rs864309679(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

17726876

Gene

NHS

is a	snp
is	mentioned by
dbSNP	rs864309679
dbSNP (classic)	rs864309679
ClinGen	rs864309679
ebi	rs864309679
HLI	rs864309679
Exac	rs864309679
Gnomad	rs864309679
Varsome	rs864309679
LitVar	rs864309679
Map	rs864309679
PheGenI	rs864309679
Biobank	rs864309679
1000 genomes	rs864309679
hgdp	rs864309679
ensembl	rs864309679
geneview	rs864309679
scholar	rs864309679
google	rs864309679
pharmgkb	rs864309679
gwascentral	rs864309679
openSNP	rs864309679
23andMe	rs864309679
SNPshot	rs864309679
SNPdbe	rs864309679
MSV3d	rs864309679
GWAS Ctlg	rs864309679

Max Magnitude

0

ClinVar
Risk	rs864309679(-;-)
Alt	rs864309679(-;-)
Reference	Rs864309679(G;G)
Significance	Pathogenic
Disease	Congenital cataract
Variation	info
Gene	NHS
CLNDBN	Congenital cataract
Reversed	0
HGVS	NC_000023.10:g.17744996delG
CLNSRC
CLNACC	RCV000203327.1,