rs886039869

Orientation

plus

Stabilized

plus

Make rs886039869(C;C)

Make rs886039869(C;T)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

196740786

Gene

CFH

is a	snp
is	mentioned by
dbSNP	rs886039869
dbSNP (classic)	rs886039869
ClinGen	rs886039869
ebi	rs886039869
HLI	rs886039869
Exac	rs886039869
Gnomad	rs886039869
Varsome	rs886039869
LitVar	rs886039869
Map	rs886039869
PheGenI	rs886039869
Biobank	rs886039869
1000 genomes	rs886039869
hgdp	rs886039869
ensembl	rs886039869
geneview	rs886039869
scholar	rs886039869
google	rs886039869
pharmgkb	rs886039869
gwascentral	rs886039869
openSNP	rs886039869
23andMe	rs886039869
SNPshot	rs886039869
SNPdbe	rs886039869
MSV3d	rs886039869
GWAS Ctlg	rs886039869

Max Magnitude

0

ClinVar
Risk	rs886039869(C;C)
Alt	rs886039869(C;C)
Reference	Rs886039869(T;T)
Significance	Probable-Pathogenic
Disease	Atypical hemolytic-uremic syndrome 1
Variation	info
Gene	CFH
CLNDBN	Atypical hemolytic-uremic syndrome 1
Reversed	0
HGVS	NC_000001.10:g.196709916T>C
CLNSRC
CLNACC	RCV000256395.1,