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rs267606878

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606878(C;T)
Make rs267606878(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position104703439
GeneINF2
is asnp
is mentioned by
dbSNPrs267606878
ebirs267606878
HLIrs267606878
Exacrs267606878
Varsomers267606878
Maprs267606878
PheGenIrs267606878
hapmaprs267606878
1000 genomesrs267606878
hgdprs267606878
ensemblrs267606878
gopubmedrs267606878
geneviewrs267606878
scholarrs267606878
googlers267606878
pharmgkbrs267606878
gwascentralrs267606878
openSNPrs267606878
23andMers267606878
23andMe allrs267606878
SNP Nexus

SNPshotrs267606878
SNPdbers267606878
MSV3drs267606878
GWAS Ctlgrs267606878
Max Magnitude0
ClinVar
Risk rs267606878(T;T)
Alt rs267606878(T;T)
Reference rs267606878(C;C)
Significance Pathogenic
Disease Focal segmental glomerulosclerosis 5
Variation info
Gene INF2
CLNDBN Focal segmental glomerulosclerosis 5
Reversed 0
HGVS NC_000014.8:g.105169776C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000001107.2,