rs398122979

Orientation

minus

Stabilized

minus

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

Make rs398122979(A;G)

Make rs398122979(G;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

40702636

Gene

COQ8B

is a	snp
is	mentioned by
dbSNP	rs398122979
dbSNP (classic)	rs398122979
ClinGen	rs398122979
ebi	rs398122979
HLI	rs398122979
Exac	rs398122979
Gnomad	rs398122979
Varsome	rs398122979
LitVar	rs398122979
Map	rs398122979
PheGenI	rs398122979
Biobank	rs398122979
1000 genomes	rs398122979
hgdp	rs398122979
ensembl	rs398122979
geneview	rs398122979
scholar	rs398122979
google	rs398122979
pharmgkb	rs398122979
gwascentral	rs398122979
openSNP	rs398122979
23andMe	rs398122979
SNPshot	rs398122979
SNPdbe	rs398122979
MSV3d	rs398122979
GWAS Ctlg	rs398122979

Max Magnitude

0

ClinVar
Risk	rs398122979(G;G)
Alt	rs398122979(G;G)
Reference	Rs398122979(A;A)
Significance	Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	COQ8B ADCK4
CLNDBN	Nephrotic syndrome, type 9
Reversed	1
HGVS	NC_000019.9:g.41208541T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000077754.4,