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rs766898395

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs766898395(-;-)
Make rs766898395(-;T)
Make rs766898395(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position105604483
GeneFKTN
is asnp
is mentioned by
dbSNPrs766898395
ebirs766898395
HLIrs766898395
Exacrs766898395
Varsomers766898395
Maprs766898395
PheGenIrs766898395
hapmaprs766898395
1000 genomesrs766898395
hgdprs766898395
ensemblrs766898395
gopubmedrs766898395
geneviewrs766898395
scholarrs766898395
googlers766898395
pharmgkbrs766898395
gwascentralrs766898395
openSNPrs766898395
23andMers766898395
23andMe allrs766898395
SNP Nexus

SNPshotrs766898395
SNPdbers766898395
MSV3drs766898395
GWAS Ctlgrs766898395
Max Magnitude0
ClinVar
Risk rs766898395(T;T)
Alt rs766898395(T;T)
Reference rs766898395(;)
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
CLNACC RCV000079438.5, RCV000169031.1,