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rs869025330

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025330(A;G)
Make rs869025330(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position108586609
GeneCOL4A5
is asnp
is mentioned by
dbSNPrs869025330
ebirs869025330
HLIrs869025330
Exacrs869025330
Varsomers869025330
Maprs869025330
PheGenIrs869025330
hapmaprs869025330
1000 genomesrs869025330
hgdprs869025330
ensemblrs869025330
gopubmedrs869025330
geneviewrs869025330
scholarrs869025330
googlers869025330
pharmgkbrs869025330
gwascentralrs869025330
openSNPrs869025330
23andMers869025330
23andMe allrs869025330
SNP Nexus

SNPshotrs869025330
SNPdbers869025330
MSV3drs869025330
GWAS Ctlgrs869025330
Max Magnitude0
ClinVar
Risk rs869025330(G;G)
Alt rs869025330(G;G)
Reference rs869025330(A;A)
Significance Probable-Pathogenic
Disease Alport syndrome
Variation info
Gene COL4A5
CLNDBN Alport syndrome, X-linked recessive
Reversed 0
HGVS NC_000023.10:g.107829839A>G
CLNSRC
CLNACC RCV000207933.1,