rs398123283

Orientation

minus

Stabilized

minus

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

Make rs398123283(C;T)

Make rs398123283(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

43958537

Gene

NDP

is a	snp
is	mentioned by
dbSNP	rs398123283
dbSNP (classic)	rs398123283
ClinGen	rs398123283
ebi	rs398123283
HLI	rs398123283
Exac	rs398123283
Gnomad	rs398123283
Varsome	rs398123283
LitVar	rs398123283
Map	rs398123283
PheGenI	rs398123283
Biobank	rs398123283
1000 genomes	rs398123283
hgdp	rs398123283
ensembl	rs398123283
geneview	rs398123283
scholar	rs398123283
google	rs398123283
pharmgkb	rs398123283
gwascentral	rs398123283
openSNP	rs398123283
23andMe	rs398123283
SNPshot	rs398123283
SNPdbe	rs398123283
MSV3d	rs398123283
GWAS Ctlg	rs398123283

Max Magnitude

0

ClinVar
Risk	rs398123283(T;T)
Alt	rs398123283(T;T)
Reference	Rs398123283(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	NDP
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.43817783G>A
CLNSRC	HGMD
CLNACC	RCV000078465.4,