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rs797045035

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045035(A;A)
Make rs797045035(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position108680884
GeneCOL4A5
is asnp
is mentioned by
dbSNPrs797045035
ebirs797045035
HLIrs797045035
Exacrs797045035
Varsomers797045035
Maprs797045035
PheGenIrs797045035
hapmaprs797045035
1000 genomesrs797045035
hgdprs797045035
ensemblrs797045035
gopubmedrs797045035
geneviewrs797045035
scholarrs797045035
googlers797045035
pharmgkbrs797045035
gwascentralrs797045035
openSNPrs797045035
23andMers797045035
23andMe allrs797045035
SNP Nexus

SNPshotrs797045035
SNPdbers797045035
MSV3drs797045035
GWAS Ctlgrs797045035
Max Magnitude0
ClinVar
Risk rs797045035(A;A)
Alt rs797045035(A;A)
Reference rs797045035(G;G)
Significance Pathogenic
Disease Alport syndrome
Variation info
Gene COL4A5
CLNDBN Alport syndrome, X-linked recessive
Reversed 0
HGVS NC_000023.10:g.107924114G>A
CLNSRC Baylor College of Medicine
CLNACC RCV000191073.1,