rs386134151

Orientation

minus

Stabilized

minus

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

Make rs386134151(-;T)

Make rs386134151(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

149182048

Gene

CP

is a	snp
is	mentioned by
dbSNP	rs386134151
dbSNP (classic)	rs386134151
ClinGen	rs386134151
ebi	rs386134151
HLI	rs386134151
Exac	rs386134151
Gnomad	rs386134151
Varsome	rs386134151
LitVar	rs386134151
Map	rs386134151
PheGenI	rs386134151
Biobank	rs386134151
1000 genomes	rs386134151
hgdp	rs386134151
ensembl	rs386134151
geneview	rs386134151
scholar	rs386134151
google	rs386134151
pharmgkb	rs386134151
gwascentral	rs386134151
openSNP	rs386134151
23andMe	rs386134151
SNPshot	rs386134151
SNPdbe	rs386134151
MSV3d	rs386134151
GWAS Ctlg	rs386134151

Merged from

Rs587777923

Max Magnitude

0

ClinVar
Risk	rs386134151(T;T)
Alt	rs386134151(T;T)
Reference	Rs386134151(-;-)
Significance	Pathogenic
Disease	Deficiency of ferroxidase
Variation	info
Gene	CP
CLNDBN	Deficiency of ferroxidase
Reversed	1
HGVS	NC_000003.11:g.148899835dupA
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034978.1,