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rs587776402

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776402(A;A)
Make rs587776402(A;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position108686030
GeneCOL4A5
is asnp
is mentioned by
dbSNPrs587776402
ebirs587776402
HLIrs587776402
Exacrs587776402
Varsomers587776402
Maprs587776402
PheGenIrs587776402
hapmaprs587776402
1000 genomesrs587776402
hgdprs587776402
ensemblrs587776402
gopubmedrs587776402
geneviewrs587776402
scholarrs587776402
googlers587776402
pharmgkbrs587776402
gwascentralrs587776402
openSNPrs587776402
23andMers587776402
23andMe allrs587776402
SNP Nexus

SNPshotrs587776402
SNPdbers587776402
MSV3drs587776402
GWAS Ctlgrs587776402
Max Magnitude0
ClinVar
Risk rs587776402(A;A)
Alt rs587776402(A;A)
Reference rs587776402(G;G)
Significance Pathogenic
Disease Alport syndrome
Variation info
Gene COL4A5
CLNDBN Alport syndrome, X-linked recessive
Reversed 0
HGVS NC_000023.10:g.107929260G>A
CLNSRC ARUP COL4A5
CLNACC RCV000021593.1,