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rs267606877

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606877(C;C)
Make rs267606877(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position104703343
GeneINF2
is asnp
is mentioned by
dbSNPrs267606877
ebirs267606877
HLIrs267606877
Exacrs267606877
Varsomers267606877
Maprs267606877
PheGenIrs267606877
hapmaprs267606877
1000 genomesrs267606877
hgdprs267606877
ensemblrs267606877
gopubmedrs267606877
geneviewrs267606877
scholarrs267606877
googlers267606877
pharmgkbrs267606877
gwascentralrs267606877
openSNPrs267606877
23andMers267606877
23andMe allrs267606877
SNP Nexus

SNPshotrs267606877
SNPdbers267606877
MSV3drs267606877
GWAS Ctlgrs267606877
Max Magnitude0
ClinVar
Risk rs267606877(C;C)
Alt rs267606877(C;C)
Reference rs267606877(T;T)
Significance Pathogenic
Disease Focal segmental glomerulosclerosis 5
Variation info
Gene INF2
CLNDBN Focal segmental glomerulosclerosis 5
Reversed 0
HGVS NC_000014.8:g.105169680T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001105.2,