rs121913063

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common genotype

Make rs121913063(G;T)

Make rs121913063(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

196747209

Gene

CFH

is a	snp
is	mentioned by
dbSNP	rs121913063
dbSNP (classic)	rs121913063
ClinGen	rs121913063
ebi	rs121913063
HLI	rs121913063
Exac	rs121913063
Gnomad	rs121913063
Varsome	rs121913063
LitVar	rs121913063
Map	rs121913063
PheGenI	rs121913063
Biobank	rs121913063
1000 genomes	rs121913063
hgdp	rs121913063
ensembl	rs121913063
geneview	rs121913063
scholar	rs121913063
google	rs121913063
pharmgkb	rs121913063
gwascentral	rs121913063
openSNP	rs121913063
23andMe	rs121913063
SNPshot	rs121913063
SNPdbe	rs121913063
MSV3d	rs121913063
GWAS Ctlg	rs121913063

Max Magnitude

0

OMIM	134370
Desc
Variant	0022
Related	also

ClinVar
Risk	rs121913063(T;T)
Alt	rs121913063(T;T)
Reference	Rs121913063(G;G)
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.196716339G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018031.5,