rs121913060

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common genotype

Make rs121913060(G;T)

Make rs121913060(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

196747131

Gene

CFH

is a	snp
is	mentioned by
dbSNP	rs121913060
dbSNP (classic)	rs121913060
ClinGen	rs121913060
ebi	rs121913060
HLI	rs121913060
Exac	rs121913060
Gnomad	rs121913060
Varsome	rs121913060
LitVar	rs121913060
Map	rs121913060
PheGenI	rs121913060
Biobank	rs121913060
1000 genomes	rs121913060
hgdp	rs121913060
ensembl	rs121913060
geneview	rs121913060
scholar	rs121913060
google	rs121913060
pharmgkb	rs121913060
gwascentral	rs121913060
openSNP	rs121913060
23andMe	rs121913060
SNPshot	rs121913060
SNPdbe	rs121913060
MSV3d	rs121913060
GWAS Ctlg	rs121913060

Max Magnitude

0

OMIM	134370
Desc
Variant	0018
Related	also

ClinVar
Risk	rs121913060(T;T)
Alt	rs121913060(T;T)
Reference	Rs121913060(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.196716261G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018027.4,