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rs137854486

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137854486(A;A)
Make rs137854486(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position215376612
GeneFN1
is asnp
is mentioned by
dbSNPrs137854486
ebirs137854486
HLIrs137854486
Exacrs137854486
Varsomers137854486
Maprs137854486
PheGenIrs137854486
hapmaprs137854486
1000 genomesrs137854486
hgdprs137854486
ensemblrs137854486
gopubmedrs137854486
geneviewrs137854486
scholarrs137854486
googlers137854486
pharmgkbrs137854486
gwascentralrs137854486
openSNPrs137854486
23andMers137854486
23andMe allrs137854486
SNP Nexus

SNPshotrs137854486
SNPdbers137854486
MSV3drs137854486
GWAS Ctlgrs137854486
Max Magnitude0
OMIM135600
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137854486(A;A)
Alt rs137854486(A;A)
Reference rs137854486(T;T)
Significance Pathogenic
Disease Glomerulopathy with fibronectin deposits 2
Variation info
Gene FN1
CLNDBN Glomerulopathy with fibronectin deposits 2
Reversed 1
HGVS NC_000002.11:g.216241335A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017720.27,