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rs1064796797

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome3
Position58145949
GeneFLNB
is asnp
is mentioned by
dbSNPrs1064796797
dbSNP (old)rs1064796797
ClinGenrs1064796797
ebirs1064796797
HLIrs1064796797
Exacrs1064796797
Gnomadrs1064796797
Varsomers1064796797
Maprs1064796797
PheGenIrs1064796797
Biobankrs1064796797
1000 genomesrs1064796797
hgdprs1064796797
ensemblrs1064796797
gopubmedrs1064796797
geneviewrs1064796797
scholarrs1064796797
googlers1064796797
pharmgkbrs1064796797
gwascentralrs1064796797
openSNPrs1064796797
23andMers1064796797
23andMe allrs1064796797
SNPshotrs1064796797
SNPdbers1064796797
MSV3drs1064796797
GWAS Ctlgrs1064796797
Max Magnitude0
ClinVar
Risk rs1064796797(A;A)
Alt rs1064796797(A;A)
Reference Rs1064796797(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FLNB
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.58131676C>A
CLNSRC
CLNACC RCV000486409.1,