Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606879

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606879(A;A)
Make rs267606879(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position104703428
GeneINF2
is asnp
is mentioned by
dbSNPrs267606879
ebirs267606879
HLIrs267606879
Exacrs267606879
Varsomers267606879
Maprs267606879
PheGenIrs267606879
hapmaprs267606879
1000 genomesrs267606879
hgdprs267606879
ensemblrs267606879
gopubmedrs267606879
geneviewrs267606879
scholarrs267606879
googlers267606879
pharmgkbrs267606879
gwascentralrs267606879
openSNPrs267606879
23andMers267606879
23andMe allrs267606879
SNP Nexus

SNPshotrs267606879
SNPdbers267606879
MSV3drs267606879
GWAS Ctlgrs267606879
Max Magnitude0
ClinVar
Risk rs267606879(A;A)
Alt rs267606879(A;A)
Reference rs267606879(G;G)
Significance Pathogenic
Disease Focal segmental glomerulosclerosis 5
Variation info
Gene INF2
CLNDBN Focal segmental glomerulosclerosis 5
Reversed 0
HGVS NC_000014.8:g.105169765G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001108.2,