rs267606803

Orientation

minus

Stabilized

minus

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

Make rs267606803(A;A)

Make rs267606803(A;T)

Reference

GRCh38 38.1/141

Chromosome

18

Position

57550760

Gene

FECH

is a	snp
is	mentioned by
dbSNP	rs267606803
dbSNP (classic)	rs267606803
ClinGen	rs267606803
ebi	rs267606803
HLI	rs267606803
Exac	rs267606803
Gnomad	rs267606803
Varsome	rs267606803
LitVar	rs267606803
Map	rs267606803
PheGenI	rs267606803
Biobank	rs267606803
1000 genomes	rs267606803
hgdp	rs267606803
ensembl	rs267606803
geneview	rs267606803
scholar	rs267606803
google	rs267606803
pharmgkb	rs267606803
gwascentral	rs267606803
openSNP	rs267606803
23andMe	rs267606803
SNPshot	rs267606803
SNPdbe	rs267606803
MSV3d	rs267606803
GWAS Ctlg	rs267606803

Max Magnitude

0

ClinVar
Risk	rs267606803(A;A)
Alt	rs267606803(A;A)
Reference	Rs267606803(T;T)
Significance	Pathogenic
Disease	Erythropoietic protoporphyria
Variation	info
Gene	FECH
CLNDBN	Erythropoietic protoporphyria
Reversed	1
HGVS	NC_000018.9:g.55217992A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000591.3,