rs386134156

Orientation

minus

Stabilized

minus

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

Make rs386134156(C;T)

Make rs386134156(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

149178592

Gene

CP

is a	snp
is	mentioned by
dbSNP	rs386134156
dbSNP (classic)	rs386134156
ClinGen	rs386134156
ebi	rs386134156
HLI	rs386134156
Exac	rs386134156
Gnomad	rs386134156
Varsome	rs386134156
LitVar	rs386134156
Map	rs386134156
PheGenI	rs386134156
Biobank	rs386134156
1000 genomes	rs386134156
hgdp	rs386134156
ensembl	rs386134156
geneview	rs386134156
scholar	rs386134156
google	rs386134156
pharmgkb	rs386134156
gwascentral	rs386134156
openSNP	rs386134156
23andMe	rs386134156
SNPshot	rs386134156
SNPdbe	rs386134156
MSV3d	rs386134156
GWAS Ctlg	rs386134156

Max Magnitude

0

ClinVar
Risk	rs386134156(T;T)
Alt	rs386134156(T;T)
Reference	Rs386134156(C;C)
Significance	Pathogenic
Disease	Deficiency of ferroxidase
Variation	info
Gene	CP
CLNDBN	Deficiency of ferroxidase
Reversed	1
HGVS	NC_000003.11:g.148896379G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034951.2,