rs796052138

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AGA;AGA)	0	common in clinvar

Make rs796052138(-;-)

Make rs796052138(-;AGA)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

196679674

Gene

CFH

is a	snp
is	mentioned by
dbSNP	rs796052138
dbSNP (classic)	rs796052138
ClinGen	rs796052138
ebi	rs796052138
HLI	rs796052138
Exac	rs796052138
Gnomad	rs796052138
Varsome	rs796052138
LitVar	rs796052138
Map	rs796052138
PheGenI	rs796052138
Biobank	rs796052138
1000 genomes	rs796052138
hgdp	rs796052138
ensembl	rs796052138
geneview	rs796052138
scholar	rs796052138
google	rs796052138
pharmgkb	rs796052138
gwascentral	rs796052138
openSNP	rs796052138
23andMe	rs796052138
SNPshot	rs796052138
SNPdbe	rs796052138
MSV3d	rs796052138
GWAS Ctlg	rs796052138

Max Magnitude

0

ClinVar
Risk	rs796052138(-;-)
Alt	rs796052138(-;-)
Reference	Rs796052138(AGA;AGA)
Significance	Pathogenic
Disease	Factor H deficiency
Variation	info
Gene	CFH
CLNDBN	Factor H deficiency
Reversed	0
HGVS	NC_000001.10:g.196648804_196648806delAGA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018022.29,