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rs267606880

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606880(C;C)
Make rs267606880(C;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position104701490
GeneINF2
is asnp
is mentioned by
dbSNPrs267606880
ebirs267606880
HLIrs267606880
Exacrs267606880
Varsomers267606880
Maprs267606880
PheGenIrs267606880
hapmaprs267606880
1000 genomesrs267606880
hgdprs267606880
ensemblrs267606880
gopubmedrs267606880
geneviewrs267606880
scholarrs267606880
googlers267606880
pharmgkbrs267606880
gwascentralrs267606880
openSNPrs267606880
23andMers267606880
23andMe allrs267606880
SNP Nexus

SNPshotrs267606880
SNPdbers267606880
MSV3drs267606880
GWAS Ctlgrs267606880
Max Magnitude0
ClinVar
Risk rs267606880(C;C)
Alt rs267606880(C;C)
Reference rs267606880(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.105167827T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001109.2,