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rs878853114

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853114(A;A)
Make rs878853114(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position108591232
GeneCOL4A5
is asnp
is mentioned by
dbSNPrs878853114
ebirs878853114
HLIrs878853114
Exacrs878853114
Varsomers878853114
Maprs878853114
PheGenIrs878853114
hapmaprs878853114
1000 genomesrs878853114
hgdprs878853114
ensemblrs878853114
gopubmedrs878853114
geneviewrs878853114
scholarrs878853114
googlers878853114
pharmgkbrs878853114
gwascentralrs878853114
openSNPrs878853114
23andMers878853114
23andMe allrs878853114
SNP Nexus

SNPshotrs878853114
SNPdbers878853114
MSV3drs878853114
GWAS Ctlgrs878853114
Max Magnitude0
ClinVar
Risk rs878853114(A;A)
Alt rs878853114(A;A)
Reference rs878853114(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COL4A5
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.107834462G>A
CLNSRC
CLNACC RCV000224182.1,