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rs878853089

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853089(A;A)
Make rs878853089(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position108621848
GeneCOL4A5
is asnp
is mentioned by
dbSNPrs878853089
ebirs878853089
HLIrs878853089
Exacrs878853089
Varsomers878853089
Maprs878853089
PheGenIrs878853089
hapmaprs878853089
1000 genomesrs878853089
hgdprs878853089
ensemblrs878853089
gopubmedrs878853089
geneviewrs878853089
scholarrs878853089
googlers878853089
pharmgkbrs878853089
gwascentralrs878853089
openSNPrs878853089
23andMers878853089
23andMe allrs878853089
SNP Nexus

SNPshotrs878853089
SNPdbers878853089
MSV3drs878853089
GWAS Ctlgrs878853089
Max Magnitude0
ClinVar
Risk rs878853089(A;A)
Alt rs878853089(A;A)
Reference rs878853089(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL4A5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.107865078G>A
CLNSRC
CLNACC RCV000224889.1,