rs150146721

Orientation

plus

Stabilized

plus

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

Make rs150146721(A;A)

Make rs150146721(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

57554336

Gene

FECH

is a	snp
is	mentioned by
dbSNP	rs150146721
dbSNP (classic)	rs150146721
ClinGen	rs150146721
ebi	rs150146721
HLI	rs150146721
Exac	rs150146721
Gnomad	rs150146721
Varsome	rs150146721
LitVar	rs150146721
Map	rs150146721
PheGenI	rs150146721
Biobank	rs150146721
1000 genomes	rs150146721
hgdp	rs150146721
ensembl	rs150146721
geneview	rs150146721
scholar	rs150146721
google	rs150146721
pharmgkb	rs150146721
gwascentral	rs150146721
openSNP	rs150146721
23andMe	rs150146721
SNPshot	rs150146721
SNPdbe	rs150146721
MSV3d	rs150146721
GWAS Ctlg	rs150146721

Max Magnitude

0

ClinVar
Risk	rs150146721(A;A)
Alt	rs150146721(A;A)
Reference	Rs150146721(G;G)
Significance	Probable-Pathogenic
Disease	Erythropoietic protoporphyria
Variation	info
Gene	FECH
CLNDBN	Erythropoietic protoporphyria
Reversed	0
HGVS	NC_000018.9:g.55221568G>A
CLNSRC
CLNACC	RCV000416464.1,