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rs267607207

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607207(A;A)
Make rs267607207(A;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position49123216
GeneLAMB2
is asnp
is mentioned by
dbSNPrs267607207
ebirs267607207
HLIrs267607207
Exacrs267607207
Varsomers267607207
Maprs267607207
PheGenIrs267607207
hapmaprs267607207
1000 genomesrs267607207
hgdprs267607207
ensemblrs267607207
gopubmedrs267607207
geneviewrs267607207
scholarrs267607207
googlers267607207
pharmgkbrs267607207
gwascentralrs267607207
openSNPrs267607207
23andMers267607207
23andMe allrs267607207
SNP Nexus

SNPshotrs267607207
SNPdbers267607207
MSV3drs267607207
GWAS Ctlgrs267607207
Max Magnitude0
ClinVar
Risk rs267607207(A;A)
Alt rs267607207(A;A)
Reference rs267607207(C;C)
Significance Pathogenic
Disease Nephrotic syndrome
Variation info
Gene LAMB2
CLNDBN Nephrotic syndrome, type 5, with or without ocular abnormalities
Reversed 1
HGVS NC_000003.11:g.49160649G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015634.21,