rs267606804

Orientation

minus

Stabilized

minus

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

Make rs267606804(C;T)

Make rs267606804(T;T)

Reference

GRCh38 38.1/141

Chromosome

18

Position

57550759

Gene

FECH

is a	snp
is	mentioned by
dbSNP	rs267606804
dbSNP (classic)	rs267606804
ClinGen	rs267606804
ebi	rs267606804
HLI	rs267606804
Exac	rs267606804
Gnomad	rs267606804
Varsome	rs267606804
LitVar	rs267606804
Map	rs267606804
PheGenI	rs267606804
Biobank	rs267606804
1000 genomes	rs267606804
hgdp	rs267606804
ensembl	rs267606804
geneview	rs267606804
scholar	rs267606804
google	rs267606804
pharmgkb	rs267606804
gwascentral	rs267606804
openSNP	rs267606804
23andMe	rs267606804
SNPshot	rs267606804
SNPdbe	rs267606804
MSV3d	rs267606804
GWAS Ctlg	rs267606804

Max Magnitude

0

ClinVar
Risk	rs267606804(T;T)
Alt	rs267606804(T;T)
Reference	Rs267606804(C;C)
Significance	Pathogenic
Disease	Erythropoietic protoporphyria
Variation	info
Gene	FECH
CLNDBN	Erythropoietic protoporphyria
Reversed	1
HGVS	NC_000018.9:g.55217991G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000591.3,