rs121913051

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common genotype

Make rs121913051(C;G)

Make rs121913051(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

196747260

Gene

CFH

is a	snp
is	mentioned by
dbSNP	rs121913051
dbSNP (classic)	rs121913051
ClinGen	rs121913051
ebi	rs121913051
HLI	rs121913051
Exac	rs121913051
Gnomad	rs121913051
Varsome	rs121913051
LitVar	rs121913051
Map	rs121913051
PheGenI	rs121913051
Biobank	rs121913051
1000 genomes	rs121913051
hgdp	rs121913051
ensembl	rs121913051
geneview	rs121913051
scholar	rs121913051
google	rs121913051
pharmgkb	rs121913051
gwascentral	rs121913051
openSNP	rs121913051
23andMe	rs121913051
SNPshot	rs121913051
SNPdbe	rs121913051
MSV3d	rs121913051
GWAS Ctlg	rs121913051

Max Magnitude

0

OMIM	134370
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121913051(G;G) rs121913051(T;T)
Alt	rs121913051(G;G) rs121913051(T;T)
Reference	Rs121913051(C;C)
Significance	Other
Disease	Atypical hemolytic-uremic syndrome 1 CFH-Related Disorders
Variation	info
Gene	CFH
CLNDBN	Atypical hemolytic-uremic syndrome 1 CFH-Related Disorders
Reversed	0
HGVS	NC_000001.10:g.196716390C>G; NC_000001.10:g.196716390C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018008.2, RCV000276556.1,