Have questions? Visit https://www.reddit.com/r/SNPedia

rs397515491

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515491(-;-)
Make rs397515491(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position108580532
GeneCOL4A5
is asnp
is mentioned by
dbSNPrs397515491
ebirs397515491
HLIrs397515491
Exacrs397515491
Varsomers397515491
Maprs397515491
PheGenIrs397515491
hapmaprs397515491
1000 genomesrs397515491
hgdprs397515491
ensemblrs397515491
gopubmedrs397515491
geneviewrs397515491
scholarrs397515491
googlers397515491
pharmgkbrs397515491
gwascentralrs397515491
openSNPrs397515491
23andMers397515491
23andMe allrs397515491
SNP Nexus

SNPshotrs397515491
SNPdbers397515491
MSV3drs397515491
GWAS Ctlgrs397515491
Max Magnitude0
ClinVar
Risk rs397515491(;)
Alt rs397515491(;)
Reference rs397515491(G;G)
Significance Pathogenic
Disease Alport syndrome
Variation info
Gene COL4A5
CLNDBN Alport syndrome, X-linked recessive
Reversed 0
HGVS NC_000023.10:g.107823762delG
CLNSRC
CLNACC RCV000021198.1,