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rs202128397

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs202128397(C;T)
Make rs202128397(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position123370935
GeneCRB2
is asnp
is mentioned by
dbSNPrs202128397
ebirs202128397
HLIrs202128397
Exacrs202128397
Varsomers202128397
Maprs202128397
PheGenIrs202128397
hapmaprs202128397
1000 genomesrs202128397
hgdprs202128397
ensemblrs202128397
gopubmedrs202128397
geneviewrs202128397
scholarrs202128397
googlers202128397
pharmgkbrs202128397
gwascentralrs202128397
openSNPrs202128397
23andMers202128397
23andMe allrs202128397
SNP Nexus

SNPshotrs202128397
SNPdbers202128397
MSV3drs202128397
GWAS Ctlgrs202128397
Max Magnitude0
ClinVar
Risk rs202128397(T;T)
Alt rs202128397(T;T)
Reference rs202128397(C;C)
Significance Pathogenic
Disease Focal segmental glomerulosclerosis 9
Variation info
Gene CRB2
CLNDBN Focal segmental glomerulosclerosis 9
Reversed 0
HGVS NC_000009.11:g.126133214C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000157655.3,