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rs869025198

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025198(C;C)
Make rs869025198(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position215376610
GeneFN1
is asnp
is mentioned by
dbSNPrs869025198
ebirs869025198
HLIrs869025198
Exacrs869025198
Varsomers869025198
Maprs869025198
PheGenIrs869025198
hapmaprs869025198
1000 genomesrs869025198
hgdprs869025198
ensemblrs869025198
gopubmedrs869025198
geneviewrs869025198
scholarrs869025198
googlers869025198
pharmgkbrs869025198
gwascentralrs869025198
openSNPrs869025198
23andMers869025198
23andMe allrs869025198
SNP Nexus

SNPshotrs869025198
SNPdbers869025198
MSV3drs869025198
GWAS Ctlgrs869025198
Max Magnitude0
ClinVar
Risk rs869025198(C;C)
Alt rs869025198(C;C)
Reference rs869025198(G;G)
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.216241333C>G
CLNSRC
CLNACC RCV000207361.1,