rs121913055

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common genotype

Make rs121913055(G;G)

Make rs121913055(G;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

196747183

Gene

CFH

is a	snp
is	mentioned by
dbSNP	rs121913055
dbSNP (classic)	rs121913055
ClinGen	rs121913055
ebi	rs121913055
HLI	rs121913055
Exac	rs121913055
Gnomad	rs121913055
Varsome	rs121913055
LitVar	rs121913055
Map	rs121913055
PheGenI	rs121913055
Biobank	rs121913055
1000 genomes	rs121913055
hgdp	rs121913055
ensembl	rs121913055
geneview	rs121913055
scholar	rs121913055
google	rs121913055
pharmgkb	rs121913055
gwascentral	rs121913055
openSNP	rs121913055
23andMe	rs121913055
SNPshot	rs121913055
SNPdbe	rs121913055
MSV3d	rs121913055
GWAS Ctlg	rs121913055

Max Magnitude

0

OMIM	134370
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121913055(G;G)
Alt	rs121913055(G;G)
Reference	Rs121913055(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.196716313T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018014.3,