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rs878853030

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853030(-;-)
Make rs878853030(-;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position108692768
GeneCOL4A5
is asnp
is mentioned by
dbSNPrs878853030
ebirs878853030
HLIrs878853030
Exacrs878853030
Varsomers878853030
Maprs878853030
PheGenIrs878853030
hapmaprs878853030
1000 genomesrs878853030
hgdprs878853030
ensemblrs878853030
gopubmedrs878853030
geneviewrs878853030
scholarrs878853030
googlers878853030
pharmgkbrs878853030
gwascentralrs878853030
openSNPrs878853030
23andMers878853030
23andMe allrs878853030
SNP Nexus

SNPshotrs878853030
SNPdbers878853030
MSV3drs878853030
GWAS Ctlgrs878853030
Max Magnitude0
ClinVar
Risk rs878853030(;)
Alt rs878853030(;)
Reference rs878853030(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene COL4A5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.107935998delC
CLNSRC
CLNACC RCV000224452.1,