rs1057519346

Orientation

minus

Stabilized

minus

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

Make rs1057519346(-;GAC)

Make rs1057519346(GAC;GAC)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

40700388

Gene

COQ8B

is a	snp
is	mentioned by
dbSNP	rs1057519346
dbSNP (classic)	rs1057519346
ClinGen	rs1057519346
ebi	rs1057519346
HLI	rs1057519346
Exac	rs1057519346
Gnomad	rs1057519346
Varsome	rs1057519346
LitVar	rs1057519346
Map	rs1057519346
PheGenI	rs1057519346
Biobank	rs1057519346
1000 genomes	rs1057519346
hgdp	rs1057519346
ensembl	rs1057519346
geneview	rs1057519346
scholar	rs1057519346
google	rs1057519346
pharmgkb	rs1057519346
gwascentral	rs1057519346
openSNP	rs1057519346
23andMe	rs1057519346
SNPshot	rs1057519346
SNPdbe	rs1057519346
MSV3d	rs1057519346
GWAS Ctlg	rs1057519346

Max Magnitude

0

ClinVar
Risk	rs1057519346(GAC;GAC)
Alt	rs1057519346(GAC;GAC)
Reference	Rs1057519346(-;-)
Significance	Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	COQ8B ADCK4
CLNDBN	Nephrotic syndrome, type 9
Reversed	1
HGVS	NC_000019.9:g.41206294_41206296dupGTC
CLNSRC
CLNACC	RCV000416394.1,