rs587777553

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(G;G)	0	common in clinvar

Make rs587777553(A;A)

Make rs587777553(A;G)

Reference

GRCh38 38.1/142

Chromosome

17

Position

81869230

Gene

ARHGDIA

is a	snp
is	mentioned by
dbSNP	rs587777553
dbSNP (classic)	rs587777553
ClinGen	rs587777553
ebi	rs587777553
HLI	rs587777553
Exac	rs587777553
Gnomad	rs587777553
Varsome	rs587777553
LitVar	rs587777553
Map	rs587777553
PheGenI	rs587777553
Biobank	rs587777553
1000 genomes	rs587777553
hgdp	rs587777553
ensembl	rs587777553
geneview	rs587777553
scholar	rs587777553
google	rs587777553
pharmgkb	rs587777553
gwascentral	rs587777553
openSNP	rs587777553
23andMe	rs587777553
SNPshot	rs587777553
SNPdbe	rs587777553
MSV3d	rs587777553
GWAS Ctlg	rs587777553

Max Magnitude

0

ClinVar
Risk	rs587777553(A;A) Rs587777553(G;G)
Alt	rs587777553(A;A) Rs587777553(G;G)
Reference	Rs587777553(C;C)
Significance	Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	ARHGDIA
CLNDBN	Nephrotic syndrome, type 8
Reversed	1
HGVS	NC_000017.10:g.79827106G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000128809.2,