rs386134155

Orientation

minus

Stabilized

minus

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

Make rs386134155(C;T)

Make rs386134155(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

149209349

Gene

CP

is a	snp
is	mentioned by
dbSNP	rs386134155
dbSNP (classic)	rs386134155
ClinGen	rs386134155
ebi	rs386134155
HLI	rs386134155
Exac	rs386134155
Gnomad	rs386134155
Varsome	rs386134155
LitVar	rs386134155
Map	rs386134155
PheGenI	rs386134155
Biobank	rs386134155
1000 genomes	rs386134155
hgdp	rs386134155
ensembl	rs386134155
geneview	rs386134155
scholar	rs386134155
google	rs386134155
pharmgkb	rs386134155
gwascentral	rs386134155
openSNP	rs386134155
23andMe	rs386134155
SNPshot	rs386134155
SNPdbe	rs386134155
MSV3d	rs386134155
GWAS Ctlg	rs386134155

Max Magnitude

0

ClinVar
Risk	rs386134155(T;T)
Alt	rs386134155(T;T)
Reference	Rs386134155(C;C)
Significance	Pathogenic
Disease	Deficiency of ferroxidase
Variation	info
Gene	CP
CLNDBN	Deficiency of ferroxidase
Reversed	1
HGVS	NC_000003.11:g.148927136G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034949.2,