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rs587777552

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777552(A;A)
Make rs587777552(A;C)
ReferenceGRCh38 38.1/142
Chromosome17
Position81868973
GeneARHGDIA
is asnp
is mentioned by
dbSNPrs587777552
ebirs587777552
HLIrs587777552
Exacrs587777552
Varsomers587777552
Maprs587777552
PheGenIrs587777552
hapmaprs587777552
1000 genomesrs587777552
hgdprs587777552
ensemblrs587777552
gopubmedrs587777552
geneviewrs587777552
scholarrs587777552
googlers587777552
pharmgkbrs587777552
gwascentralrs587777552
openSNPrs587777552
23andMers587777552
23andMe allrs587777552
SNP Nexus

SNPshotrs587777552
SNPdbers587777552
MSV3drs587777552
GWAS Ctlgrs587777552
Max Magnitude0
ClinVar
Risk rs587777552(A,C;A,C)
Alt rs587777552(A,C;A,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,