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rs368472521

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368472521(C;T)
Make rs368472521(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position58078747
GeneFLNB
is asnp
is mentioned by
dbSNPrs368472521
dbSNP (classic)rs368472521
ClinGenrs368472521
ebirs368472521
HLIrs368472521
Exacrs368472521
Gnomadrs368472521
Varsomers368472521
LitVarrs368472521
Maprs368472521
PheGenIrs368472521
Biobankrs368472521
1000 genomesrs368472521
hgdprs368472521
ensemblrs368472521
geneviewrs368472521
scholarrs368472521
googlers368472521
pharmgkbrs368472521
gwascentralrs368472521
openSNPrs368472521
23andMers368472521
23andMe allrs368472521
SNPshotrs368472521
SNPdbers368472521
MSV3drs368472521
GWAS Ctlgrs368472521
Max Magnitude0
ClinVar
Risk rs368472521(T;T)
Alt rs368472521(T;T)
Reference Rs368472521(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FLNB
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.58064474C>T
CLNSRC
CLNACC RCV000413979.1,