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rs869025334

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025334(G;T)
Make rs869025334(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position108584503
GeneCOL4A5
is asnp
is mentioned by
dbSNPrs869025334
ebirs869025334
HLIrs869025334
Exacrs869025334
Varsomers869025334
Maprs869025334
PheGenIrs869025334
hapmaprs869025334
1000 genomesrs869025334
hgdprs869025334
ensemblrs869025334
gopubmedrs869025334
geneviewrs869025334
scholarrs869025334
googlers869025334
pharmgkbrs869025334
gwascentralrs869025334
openSNPrs869025334
23andMers869025334
23andMe allrs869025334
SNP Nexus

SNPshotrs869025334
SNPdbers869025334
MSV3drs869025334
GWAS Ctlgrs869025334
Max Magnitude0
ClinVar
Risk rs869025334(T;T)
Alt rs869025334(T;T)
Reference rs869025334(G;G)
Significance Pathogenic
Disease Alport syndrome
Variation info
Gene COL4A5
CLNDBN Alport syndrome, X-linked recessive
Reversed 0
HGVS NC_000023.10:g.107827733G>T
CLNSRC
CLNACC RCV000207794.1,