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rs398123558

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398123558(C;C)
Make rs398123558(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position105607919
GeneFKTN
is asnp
is mentioned by
dbSNPrs398123558
ebirs398123558
HLIrs398123558
Exacrs398123558
Varsomers398123558
Maprs398123558
PheGenIrs398123558
hapmaprs398123558
1000 genomesrs398123558
hgdprs398123558
ensemblrs398123558
gopubmedrs398123558
geneviewrs398123558
scholarrs398123558
googlers398123558
pharmgkbrs398123558
gwascentralrs398123558
openSNPrs398123558
23andMers398123558
23andMe allrs398123558
SNP Nexus

SNPshotrs398123558
SNPdbers398123558
MSV3drs398123558
GWAS Ctlgrs398123558
Max Magnitude0
ClinVar
Risk rs398123558(C;C)
Alt rs398123558(C;C)
Reference rs398123558(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FKTN
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.108370200T>C
CLNSRC HGMD
CLNACC RCV000079439.4,