rs372969054

Orientation

plus

Stabilized

plus

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

Make rs372969054(A;A)

Make rs372969054(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

17724365

Gene

NHS

is a	snp
is	mentioned by
dbSNP	rs372969054
dbSNP (classic)	rs372969054
ClinGen	rs372969054
ebi	rs372969054
HLI	rs372969054
Exac	rs372969054
Gnomad	rs372969054
Varsome	rs372969054
LitVar	rs372969054
Map	rs372969054
PheGenI	rs372969054
Biobank	rs372969054
1000 genomes	rs372969054
hgdp	rs372969054
ensembl	rs372969054
geneview	rs372969054
scholar	rs372969054
google	rs372969054
pharmgkb	rs372969054
gwascentral	rs372969054
openSNP	rs372969054
23andMe	rs372969054
SNPshot	rs372969054
SNPdbe	rs372969054
MSV3d	rs372969054
GWAS Ctlg	rs372969054

Max Magnitude

0

ClinVar
Risk	rs372969054(A;A)
Alt	rs372969054(A;A)
Reference	Rs372969054(G;G)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	NHS
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000023.10:g.17742485G>A
CLNSRC
CLNACC	RCV000190792.1,