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rs869025199

From SNPedia

Orientationminus
Geno Mag Summary
(CTC;CTC) 0 common in clinvar
Make rs869025199(-;-)
Make rs869025199(-;CCT)
Make rs869025199(CCT;CCT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position215386885
GeneFN1
is asnp
is mentioned by
dbSNPrs869025199
ebirs869025199
HLIrs869025199
Exacrs869025199
Varsomers869025199
Maprs869025199
PheGenIrs869025199
hapmaprs869025199
1000 genomesrs869025199
hgdprs869025199
ensemblrs869025199
gopubmedrs869025199
geneviewrs869025199
scholarrs869025199
googlers869025199
pharmgkbrs869025199
gwascentralrs869025199
openSNPrs869025199
23andMers869025199
23andMe allrs869025199
SNP Nexus

SNPshotrs869025199
SNPdbers869025199
MSV3drs869025199
GWAS Ctlgrs869025199
Max Magnitude0
ClinVar
Risk rs869025199(;)
Alt rs869025199(;)
Reference rs869025199(CTC;CTC)
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.216251608_216251610delAGG
CLNSRC
CLNACC RCV000207432.1,