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rs145784949

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs145784949(A;A)
Make rs145784949(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position149185366
GeneCP
is asnp
is mentioned by
dbSNPrs145784949
ebirs145784949
HLIrs145784949
Exacrs145784949
Varsomers145784949
Maprs145784949
PheGenIrs145784949
hapmaprs145784949
1000 genomesrs145784949
hgdprs145784949
ensemblrs145784949
gopubmedrs145784949
geneviewrs145784949
scholarrs145784949
googlers145784949
pharmgkbrs145784949
gwascentralrs145784949
openSNPrs145784949
23andMers145784949
23andMe allrs145784949
SNP Nexus

SNPshotrs145784949
SNPdbers145784949
MSV3drs145784949
GWAS Ctlgrs145784949
Max Magnitude0
ClinVar
Risk rs145784949(A;A)
Alt rs145784949(A;A)
Reference rs145784949(G;G)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 0
HGVS NC_000003.11:g.148903153G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000034950.1,