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rs878853098

From SNPedia

Orientationminus
Geno Mag Summary
(GGAGATGCTTGTG;GGAGATGCTTGTG) 0 common in clinvar
Make rs878853098(-;-)
Make rs878853098(-;GGAGATGCTTGTG)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position18786255
GeneCOMP
is asnp
is mentioned by
dbSNPrs878853098
ebirs878853098
HLIrs878853098
Exacrs878853098
Varsomers878853098
Maprs878853098
PheGenIrs878853098
hapmaprs878853098
1000 genomesrs878853098
hgdprs878853098
ensemblrs878853098
gopubmedrs878853098
geneviewrs878853098
scholarrs878853098
googlers878853098
pharmgkbrs878853098
gwascentralrs878853098
openSNPrs878853098
23andMers878853098
23andMe allrs878853098
SNP Nexus

SNPshotrs878853098
SNPdbers878853098
MSV3drs878853098
GWAS Ctlgrs878853098
Max Magnitude0
ClinVar
Risk rs878853098(;)
Alt rs878853098(;)
Reference rs878853098(GGAGATGCTTGTG;GGAGATGCTTGTG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COMP
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.18897065_18897077delCACAAGCATCTCC
CLNSRC
CLNACC RCV000224737.1,