rs587777552

Orientation

plus

Stabilized

minus

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

Make rs587777552(A;A)

Make rs587777552(A;C)

Reference

GRCh38 38.1/142

Chromosome

17

Position

81868973

Gene

ARHGDIA

is a	snp
is	mentioned by
dbSNP	rs587777552
dbSNP (classic)	rs587777552
ClinGen	rs587777552
ebi	rs587777552
HLI	rs587777552
Exac	rs587777552
Gnomad	rs587777552
Varsome	rs587777552
LitVar	rs587777552
Map	rs587777552
PheGenI	rs587777552
Biobank	rs587777552
1000 genomes	rs587777552
hgdp	rs587777552
ensembl	rs587777552
geneview	rs587777552
scholar	rs587777552
google	rs587777552
pharmgkb	rs587777552
gwascentral	rs587777552
openSNP	rs587777552
23andMe	rs587777552
SNPshot	rs587777552
SNPdbe	rs587777552
MSV3d	rs587777552
GWAS Ctlg	rs587777552

Max Magnitude

0

ClinVar
Risk	rs587777552(A;A) Rs587777552(C;C)
Alt	rs587777552(A;A) Rs587777552(C;C)
Reference	Rs587777552(G;G)
Significance	Pathogenic
Disease	Nephrotic syndrome
Variation	info
Gene	ARHGDIA
CLNDBN	Nephrotic syndrome, type 8
Reversed	1
HGVS	NC_000017.10:g.79826849C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000128808.2,