rs146899669

Orientation

plus

Stabilized

plus

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

Make rs146899669(A;C)

Make rs146899669(C;C)

Reference

GRCh38 38.1/141

Chromosome

18

Position

57550753

Gene

FECH

is a	snp
is	mentioned by
dbSNP	rs146899669
dbSNP (classic)	rs146899669
ClinGen	rs146899669
ebi	rs146899669
HLI	rs146899669
Exac	rs146899669
Gnomad	rs146899669
Varsome	rs146899669
LitVar	rs146899669
Map	rs146899669
PheGenI	rs146899669
Biobank	rs146899669
1000 genomes	rs146899669
hgdp	rs146899669
ensembl	rs146899669
geneview	rs146899669
scholar	rs146899669
google	rs146899669
pharmgkb	rs146899669
gwascentral	rs146899669
openSNP	rs146899669
23andMe	rs146899669
SNPshot	rs146899669
SNPdbe	rs146899669
MSV3d	rs146899669
GWAS Ctlg	rs146899669

Max Magnitude

0

ClinVar
Risk	rs146899669(C;C)
Alt	rs146899669(C;C)
Reference	Rs146899669(A;A)
Significance	Pathogenic
Disease	Erythropoietic protoporphyria
Variation	info
Gene	FECH
CLNDBN	Erythropoietic protoporphyria
Reversed	0
HGVS	NC_000018.9:g.55217985A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000591.3,