rs370708663

Orientation

plus

Stabilized

plus

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

Make rs370708663(C;C)

Make rs370708663(C;T)

Reference

GRCh38.p7 38.3/149

Chromosome

18

Position

57554903

Gene

FECH

is a	snp
is	mentioned by
dbSNP	rs370708663
dbSNP (classic)	rs370708663
ClinGen	rs370708663
ebi	rs370708663
HLI	rs370708663
Exac	rs370708663
Gnomad	rs370708663
Varsome	rs370708663
LitVar	rs370708663
Map	rs370708663
PheGenI	rs370708663
Biobank	rs370708663
1000 genomes	rs370708663
hgdp	rs370708663
ensembl	rs370708663
geneview	rs370708663
scholar	rs370708663
google	rs370708663
pharmgkb	rs370708663
gwascentral	rs370708663
openSNP	rs370708663
23andMe	rs370708663
SNPshot	rs370708663
SNPdbe	rs370708663
MSV3d	rs370708663
GWAS Ctlg	rs370708663

Max Magnitude

0

ClinVar
Risk	rs370708663(C;C)
Alt	rs370708663(C;C)
Reference	Rs370708663(T;T)
Significance	Probable-Pathogenic
Disease	Erythropoietic protoporphyria
Variation	info
Gene	FECH
CLNDBN	Erythropoietic protoporphyria
Reversed	0
HGVS	NC_000018.9:g.55222135T>C
CLNSRC	Illumina
CLNACC	RCV000332701.1,