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rs587777553

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777553(A;A)
Make rs587777553(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position81869230
GeneARHGDIA
is asnp
is mentioned by
dbSNPrs587777553
ebirs587777553
HLIrs587777553
Exacrs587777553
Varsomers587777553
Maprs587777553
PheGenIrs587777553
hapmaprs587777553
1000 genomesrs587777553
hgdprs587777553
ensemblrs587777553
gopubmedrs587777553
geneviewrs587777553
scholarrs587777553
googlers587777553
pharmgkbrs587777553
gwascentralrs587777553
openSNPrs587777553
23andMers587777553
23andMe allrs587777553
SNP Nexus

SNPshotrs587777553
SNPdbers587777553
MSV3drs587777553
GWAS Ctlgrs587777553
Max Magnitude0
ClinVar
Risk rs587777553(A,G;A,G)
Alt rs587777553(A,G;A,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,