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rs869025332

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025332(A;A)
Make rs869025332(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position108621866
GeneCOL4A5
is asnp
is mentioned by
dbSNPrs869025332
ebirs869025332
HLIrs869025332
Exacrs869025332
Varsomers869025332
Maprs869025332
PheGenIrs869025332
hapmaprs869025332
1000 genomesrs869025332
hgdprs869025332
ensemblrs869025332
gopubmedrs869025332
geneviewrs869025332
scholarrs869025332
googlers869025332
pharmgkbrs869025332
gwascentralrs869025332
openSNPrs869025332
23andMers869025332
23andMe allrs869025332
SNP Nexus

SNPshotrs869025332
SNPdbers869025332
MSV3drs869025332
GWAS Ctlgrs869025332
Max Magnitude0
ClinVar
Risk rs869025332(A;A)
Alt rs869025332(A;A)
Reference rs869025332(G;G)
Significance Pathogenic
Disease Alport syndrome
Variation info
Gene COL4A5
CLNDBN Alport syndrome, X-linked recessive
Reversed 0
HGVS NC_000023.10:g.107865096G>A
CLNSRC
CLNACC RCV000207888.1,