rs587777923

Merged into

rs386134151

Orientation

minus

Stabilized

minus

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

Make rs587777923(-;T)

Make rs587777923(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

149182047

Gene

CP

is a	snp
is	mentioned by
dbSNP	rs587777923
dbSNP (classic)	rs587777923
ClinGen	rs587777923
ebi	rs587777923
HLI	rs587777923
Exac	rs587777923
Gnomad	rs587777923
Varsome	rs587777923
LitVar	rs587777923
Map	rs587777923
PheGenI	rs587777923
Biobank	rs587777923
1000 genomes	rs587777923
hgdp	rs587777923
ensembl	rs587777923
geneview	rs587777923
scholar	rs587777923
google	rs587777923
pharmgkb	rs587777923
gwascentral	rs587777923
openSNP	rs587777923
23andMe	rs587777923
SNPshot	rs587777923
SNPdbe	rs587777923
MSV3d	rs587777923
GWAS Ctlg	rs587777923

Status

Merged into rs386134151

Max Magnitude

0

ClinVar
Risk	rs587777923(T;T)
Alt	rs587777923(T;T)
Reference	Rs587777923(;)
Significance	Pathogenic
Disease	Deficiency of ferroxidase
Variation	info
Gene	CP
CLNDBN	Deficiency of ferroxidase
Reversed	1
HGVS	NC_000003.11:g.148899835dupA
CLNSRC
CLNACC	RCV000034978.1,