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rs587776403

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776403(A;A)
Make rs587776403(A;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position108686130
GeneCOL4A5
is asnp
is mentioned by
dbSNPrs587776403
ebirs587776403
HLIrs587776403
Exacrs587776403
Varsomers587776403
Maprs587776403
PheGenIrs587776403
hapmaprs587776403
1000 genomesrs587776403
hgdprs587776403
ensemblrs587776403
gopubmedrs587776403
geneviewrs587776403
scholarrs587776403
googlers587776403
pharmgkbrs587776403
gwascentralrs587776403
openSNPrs587776403
23andMers587776403
23andMe allrs587776403
SNP Nexus

SNPshotrs587776403
SNPdbers587776403
MSV3drs587776403
GWAS Ctlgrs587776403
Max Magnitude0
ClinVar
Risk rs587776403(A;A)
Alt rs587776403(A;A)
Reference rs587776403(G;G)
Significance Pathogenic
Disease Alport syndrome
Variation info
Gene COL4A5
CLNDBN Alport syndrome, X-linked recessive
Reversed 0
HGVS NC_000023.10:g.107929360G>A
CLNSRC ARUP COL4A5
CLNACC RCV000021604.1,