rs397515559

Orientation

plus

Stabilized

plus

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

Make rs397515559(C;T)

Make rs397515559(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

153694783

Gene

SLC6A8

is a	snp
is	mentioned by
dbSNP	rs397515559
dbSNP (classic)	rs397515559
ClinGen	rs397515559
ebi	rs397515559
HLI	rs397515559
Exac	rs397515559
Gnomad	rs397515559
Varsome	rs397515559
LitVar	rs397515559
Map	rs397515559
PheGenI	rs397515559
Biobank	rs397515559
1000 genomes	rs397515559
hgdp	rs397515559
ensembl	rs397515559
geneview	rs397515559
scholar	rs397515559
google	rs397515559
pharmgkb	rs397515559
gwascentral	rs397515559
openSNP	rs397515559
23andMe	rs397515559
SNPshot	rs397515559
SNPdbe	rs397515559
MSV3d	rs397515559
GWAS Ctlg	rs397515559

Max Magnitude

0

ClinVar
Risk	rs397515559(T;T)
Alt	rs397515559(T;T)
Reference	Rs397515559(C;C)
Significance	Pathogenic
Disease	Creatine deficiency
Variation	info
Gene	SLC6A8
CLNDBN	Creatine deficiency, X-linked
Reversed	0
HGVS	NC_000023.10:g.152960238C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000055919.1,