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rs878853159

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853159(A;A)
Make rs878853159(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position38708128
GeneACTN4
is asnp
is mentioned by
dbSNPrs878853159
ebirs878853159
HLIrs878853159
Exacrs878853159
Varsomers878853159
Maprs878853159
PheGenIrs878853159
hapmaprs878853159
1000 genomesrs878853159
hgdprs878853159
ensemblrs878853159
gopubmedrs878853159
geneviewrs878853159
scholarrs878853159
googlers878853159
pharmgkbrs878853159
gwascentralrs878853159
openSNPrs878853159
23andMers878853159
23andMe allrs878853159
SNP Nexus

SNPshotrs878853159
SNPdbers878853159
MSV3drs878853159
GWAS Ctlgrs878853159
Max Magnitude0
ClinVar
Risk rs878853159(A;A)
Alt rs878853159(A;A)
Reference rs878853159(G;G)
Significance Pathogenic
Disease Focal segmental glomerulosclerosis 1
Variation info
Gene ACTN4
CLNDBN Focal segmental glomerulosclerosis 1
Reversed 0
HGVS NC_000019.9:g.39198768G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000224984.1,