rs587776846

Orientation

plus

Stabilized

plus

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

Make rs587776846(C;C)

Make rs587776846(C;T)

Reference

GRCh38 38.1/142

Chromosome

9

Position

121023405

Gene

C5

is a	snp
is	mentioned by
dbSNP	rs587776846
dbSNP (classic)	rs587776846
ClinGen	rs587776846
ebi	rs587776846
HLI	rs587776846
Exac	rs587776846
Gnomad	rs587776846
Varsome	rs587776846
LitVar	rs587776846
Map	rs587776846
PheGenI	rs587776846
Biobank	rs587776846
1000 genomes	rs587776846
hgdp	rs587776846
ensembl	rs587776846
geneview	rs587776846
scholar	rs587776846
google	rs587776846
pharmgkb	rs587776846
gwascentral	rs587776846
openSNP	rs587776846
23andMe	rs587776846
SNPshot	rs587776846
SNPdbe	rs587776846
MSV3d	rs587776846
GWAS Ctlg	rs587776846

Max Magnitude

0

ClinVar
Risk	rs587776846(C;C)
Alt	rs587776846(C;C)
Reference	Rs587776846(T;T)
Significance	Pathogenic
Disease	Leiner disease
Variation	info
Gene	C5
CLNDBN	Leiner disease
Reversed	0
HGVS	NC_000009.11:g.123785683T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018581.28,