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rs794727397

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727397(A;A)
Make rs794727397(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position108598766
GeneCOL4A5
is asnp
is mentioned by
dbSNPrs794727397
ebirs794727397
HLIrs794727397
Exacrs794727397
Varsomers794727397
Maprs794727397
PheGenIrs794727397
hapmaprs794727397
1000 genomesrs794727397
hgdprs794727397
ensemblrs794727397
gopubmedrs794727397
geneviewrs794727397
scholarrs794727397
googlers794727397
pharmgkbrs794727397
gwascentralrs794727397
openSNPrs794727397
23andMers794727397
23andMe allrs794727397
SNP Nexus

SNPshotrs794727397
SNPdbers794727397
MSV3drs794727397
GWAS Ctlgrs794727397
Max Magnitude0
ClinVar
Risk rs794727397(A;A)
Alt rs794727397(A;A)
Reference rs794727397(G;G)
Significance Pathogenic
Disease Alport syndrome
Variation info
Gene COL4A5
CLNDBN Alport syndrome, X-linked recessive
Reversed 0
HGVS NC_000023.10:g.107841996G>A
CLNSRC
CLNACC RCV000176533.1,