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rs1064795229

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome7
Position128844254
GeneFLNC
is asnp
is mentioned by
dbSNPrs1064795229
dbSNP (old)rs1064795229
ClinGenrs1064795229
ebirs1064795229
HLIrs1064795229
Exacrs1064795229
Gnomadrs1064795229
Varsomers1064795229
LitVarrs1064795229
Maprs1064795229
PheGenIrs1064795229
Biobankrs1064795229
1000 genomesrs1064795229
hgdprs1064795229
ensemblrs1064795229
gopubmedrs1064795229
geneviewrs1064795229
scholarrs1064795229
googlers1064795229
pharmgkbrs1064795229
gwascentralrs1064795229
openSNPrs1064795229
23andMers1064795229
23andMe allrs1064795229
SNPshotrs1064795229
SNPdbers1064795229
MSV3drs1064795229
GWAS Ctlgrs1064795229
Max Magnitude0
ClinVar
Risk rs1064795229(-;-)
Alt rs1064795229(-;-)
Reference Rs1064795229(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FLNC
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.128484308delT
CLNSRC
CLNACC RCV000483656.1,