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rs878853015

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853015(A;A)
Make rs878853015(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position108586693
GeneCOL4A5
is asnp
is mentioned by
dbSNPrs878853015
ebirs878853015
HLIrs878853015
Exacrs878853015
Varsomers878853015
Maprs878853015
PheGenIrs878853015
hapmaprs878853015
1000 genomesrs878853015
hgdprs878853015
ensemblrs878853015
gopubmedrs878853015
geneviewrs878853015
scholarrs878853015
googlers878853015
pharmgkbrs878853015
gwascentralrs878853015
openSNPrs878853015
23andMers878853015
23andMe allrs878853015
SNP Nexus

SNPshotrs878853015
SNPdbers878853015
MSV3drs878853015
GWAS Ctlgrs878853015
Max Magnitude0
ClinVar
Risk rs878853015(A;A)
Alt rs878853015(A;A)
Reference rs878853015(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL4A5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.107829923G>A
CLNSRC
CLNACC RCV000223983.1,