rs121913056

Orientation

plus

Stabilized

plus

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

Make rs121913056(A;A)

Make rs121913056(A;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

196690194

Gene

CFH

is a	snp
is	mentioned by
dbSNP	rs121913056
dbSNP (classic)	rs121913056
ClinGen	rs121913056
ebi	rs121913056
HLI	rs121913056
Exac	rs121913056
Gnomad	rs121913056
Varsome	rs121913056
LitVar	rs121913056
Map	rs121913056
PheGenI	rs121913056
Biobank	rs121913056
1000 genomes	rs121913056
hgdp	rs121913056
ensembl	rs121913056
geneview	rs121913056
scholar	rs121913056
google	rs121913056
pharmgkb	rs121913056
gwascentral	rs121913056
openSNP	rs121913056
23andMe	rs121913056
SNPshot	rs121913056
SNPdbe	rs121913056
MSV3d	rs121913056
GWAS Ctlg	rs121913056

Max Magnitude

0

OMIM	134370
Desc
Variant	0010
Related	also

ClinVar
Risk	rs121913056(A;A) rs121913056(G;G)
Alt	rs121913056(A;A) rs121913056(G;G)
Reference	Rs121913056(T;T)
Significance	Pathogenic
Disease	Factor H deficiency
Variation	info
Gene	CFH
CLNDBN	Factor H deficiency
Reversed	0
HGVS	NC_000001.10:g.196659324T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018018.29,