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rs267607183

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607183(A;A)
Make rs267607183(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position104703440
GeneINF2
is asnp
is mentioned by
dbSNPrs267607183
ebirs267607183
HLIrs267607183
Exacrs267607183
Varsomers267607183
Maprs267607183
PheGenIrs267607183
hapmaprs267607183
1000 genomesrs267607183
hgdprs267607183
ensemblrs267607183
gopubmedrs267607183
geneviewrs267607183
scholarrs267607183
googlers267607183
pharmgkbrs267607183
gwascentralrs267607183
openSNPrs267607183
23andMers267607183
23andMe allrs267607183
SNP Nexus

SNPshotrs267607183
SNPdbers267607183
MSV3drs267607183
GWAS Ctlgrs267607183
Max Magnitude0
ClinVar
Risk rs267607183(A;A)
Alt rs267607183(A;A)
Reference rs267607183(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.105169777G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001106.2,