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rs398123557

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123557(-;-)
Make rs398123557(-;T)
Make rs398123557(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position105604487
GeneFKTN
is asnp
is mentioned by
dbSNPrs398123557
ebirs398123557
HLIrs398123557
Exacrs398123557
Varsomers398123557
Maprs398123557
PheGenIrs398123557
hapmaprs398123557
1000 genomesrs398123557
hgdprs398123557
ensemblrs398123557
gopubmedrs398123557
geneviewrs398123557
scholarrs398123557
googlers398123557
pharmgkbrs398123557
gwascentralrs398123557
openSNPrs398123557
23andMers398123557
23andMe allrs398123557
SNP Nexus

SNPshotrs398123557
SNPdbers398123557
MSV3drs398123557
GWAS Ctlgrs398123557
Max Magnitude0
ClinVar
Risk rs398123557(T;T)
Alt rs398123557(T;T)
Reference rs398123557(;)
Significance Pathogenic
Disease not provided Fukuyama congenital muscular dystrophy
Variation info
Gene FKTN
CLNDBN not provided Fukuyama congenital muscular dystrophy
Reversed 0
HGVS NC_000009.11:g.108366768dupT
CLNSRC ClinVar
CLNACC RCV000079438.5, RCV000169031.1,