rs121909587

Orientation

minus

Stabilized

minus

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

Make rs121909587(C;T)

Make rs121909587(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

121050192

Gene

C5

is a	snp
is	mentioned by
dbSNP	rs121909587
dbSNP (classic)	rs121909587
ClinGen	rs121909587
ebi	rs121909587
HLI	rs121909587
Exac	rs121909587
Gnomad	rs121909587
Varsome	rs121909587
LitVar	rs121909587
Map	rs121909587
PheGenI	rs121909587
Biobank	rs121909587
1000 genomes	rs121909587
hgdp	rs121909587
ensembl	rs121909587
geneview	rs121909587
scholar	rs121909587
google	rs121909587
pharmgkb	rs121909587
gwascentral	rs121909587
openSNP	rs121909587
23andMe	rs121909587
SNPshot	rs121909587
SNPdbe	rs121909587
MSV3d	rs121909587
GWAS Ctlg	rs121909587

GMAF

0.0004591

Max Magnitude

0

OMIM	120900
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121909587(T;T)
Alt	rs121909587(T;T)
Reference	Rs121909587(C;C)
Significance	Pathogenic
Disease	Leiner disease
Variation	info
Gene	C5
CLNDBN	Leiner disease
Reversed	1
HGVS	NC_000009.11:g.123812470G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018578.27,