rs373359894

Orientation

plus

Stabilized

plus

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

Make rs373359894(A;A)

Make rs373359894(A;G)

Reference

GRCh38 38.1/142

Chromosome

9

Position

120997684

Gene

C5

is a	snp
is	mentioned by
dbSNP	rs373359894
dbSNP (classic)	rs373359894
ClinGen	rs373359894
ebi	rs373359894
HLI	rs373359894
Exac	rs373359894
Gnomad	rs373359894
Varsome	rs373359894
LitVar	rs373359894
Map	rs373359894
PheGenI	rs373359894
Biobank	rs373359894
1000 genomes	rs373359894
hgdp	rs373359894
ensembl	rs373359894
geneview	rs373359894
scholar	rs373359894
google	rs373359894
pharmgkb	rs373359894
gwascentral	rs373359894
openSNP	rs373359894
23andMe	rs373359894
SNPshot	rs373359894
SNPdbe	rs373359894
MSV3d	rs373359894
GWAS Ctlg	rs373359894

Max Magnitude

0

ClinVar
Risk	rs373359894(A;A) rs373359894(T;T)
Alt	rs373359894(A;A) rs373359894(T;T)
Reference	Rs373359894(G;G)
Significance	Other
Disease	Eculizumab
Variation	info
Gene	C5
CLNDBN	Eculizumab, poor response to
Reversed	0
HGVS	NC_000009.11:g.123759962G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000114935.4,