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rs587777741

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777741(C;T)
Make rs587777741(T;T)
ReferenceGRCh38 38.1/142
Chromosome7
Position36411062
GeneANLN
is asnp
is mentioned by
dbSNPrs587777741
ebirs587777741
HLIrs587777741
Exacrs587777741
Varsomers587777741
Maprs587777741
PheGenIrs587777741
hapmaprs587777741
1000 genomesrs587777741
hgdprs587777741
ensemblrs587777741
gopubmedrs587777741
geneviewrs587777741
scholarrs587777741
googlers587777741
pharmgkbrs587777741
gwascentralrs587777741
openSNPrs587777741
23andMers587777741
23andMe allrs587777741
SNP Nexus

SNPshotrs587777741
SNPdbers587777741
MSV3drs587777741
GWAS Ctlgrs587777741
Max Magnitude0
ClinVar
Risk rs587777741(T;T)
Alt rs587777741(T;T)
Reference rs587777741(C;C)
Significance Pathogenic
Disease Focal segmental glomerulosclerosis 8
Variation info
Gene ANLN
CLNDBN Focal segmental glomerulosclerosis 8
Reversed 0
HGVS NC_000007.13:g.36450671C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000144242.4,