rs121913057

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common genotype

Make rs121913057(A;A)

Make rs121913057(A;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

196737575

Gene

CFH

is a	snp
is	mentioned by
dbSNP	rs121913057
dbSNP (classic)	rs121913057
ClinGen	rs121913057
ebi	rs121913057
HLI	rs121913057
Exac	rs121913057
Gnomad	rs121913057
Varsome	rs121913057
LitVar	rs121913057
Map	rs121913057
PheGenI	rs121913057
Biobank	rs121913057
1000 genomes	rs121913057
hgdp	rs121913057
ensembl	rs121913057
geneview	rs121913057
scholar	rs121913057
google	rs121913057
pharmgkb	rs121913057
gwascentral	rs121913057
openSNP	rs121913057
23andMe	rs121913057
SNPshot	rs121913057
SNPdbe	rs121913057
MSV3d	rs121913057
GWAS Ctlg	rs121913057

Max Magnitude

0

OMIM	134370
Desc
Variant	0012
Related	also

ClinVar
Risk	rs121913057(A;A) rs121913057(C;C)
Alt	rs121913057(A;A) rs121913057(C;C)
Reference	Rs121913057(T;T)
Significance	Other
Disease	Atypical hemolytic-uremic syndrome 1
Variation	info
Gene	CFH
CLNDBN	Atypical hemolytic-uremic syndrome 1
Reversed	0
HGVS	NC_000001.10:g.196706705T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018020.4,