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rs119463994

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs119463994(C;C)
Make rs119463994(C;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position105604381
GeneFKTN
is asnp
is mentioned by
dbSNPrs119463994
ebirs119463994
HLIrs119463994
Exacrs119463994
Varsomers119463994
Maprs119463994
PheGenIrs119463994
hapmaprs119463994
1000 genomesrs119463994
hgdprs119463994
ensemblrs119463994
gopubmedrs119463994
geneviewrs119463994
scholarrs119463994
googlers119463994
pharmgkbrs119463994
gwascentralrs119463994
openSNPrs119463994
23andMers119463994
23andMe allrs119463994
SNP Nexus

SNPshotrs119463994
SNPdbers119463994
MSV3drs119463994
GWAS Ctlgrs119463994
Max Magnitude0
OMIM607440
Desc
Variant0011
Relatedalso
ClinVar
Risk rs119463994(C;C)
Alt rs119463994(C;C)
Reference rs119463994(G;G)
Significance Pathogenic
Disease Dilated cardiomyopathy 1X
Variation info
Gene FKTN
CLNDBN Dilated cardiomyopathy 1X
Reversed 0
HGVS NC_000009.11:g.108366662G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003365.3,