Have questions? Visit https://www.reddit.com/r/SNPedia

rs137854488

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137854488(A;G)
Make rs137854488(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position215406306
GeneFN1
is asnp
is mentioned by
dbSNPrs137854488
ebirs137854488
HLIrs137854488
Exacrs137854488
Varsomers137854488
Maprs137854488
PheGenIrs137854488
hapmaprs137854488
1000 genomesrs137854488
hgdprs137854488
ensemblrs137854488
gopubmedrs137854488
geneviewrs137854488
scholarrs137854488
googlers137854488
pharmgkbrs137854488
gwascentralrs137854488
openSNPrs137854488
23andMers137854488
23andMe allrs137854488
SNP Nexus

SNPshotrs137854488
SNPdbers137854488
MSV3drs137854488
GWAS Ctlgrs137854488
Max Magnitude0
OMIM135600
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137854488(G;G)
Alt rs137854488(G;G)
Reference rs137854488(A;A)
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.216271029T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000017722.27,