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rs863223646

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223646(-;-)
Make rs863223646(-;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154352349
GeneFLNA
is asnp
is mentioned by
dbSNPrs863223646
dbSNP (old)rs863223646
ClinGenrs863223646
ebirs863223646
HLIrs863223646
Exacrs863223646
Gnomadrs863223646
Varsomers863223646
Maprs863223646
PheGenIrs863223646
Biobankrs863223646
1000 genomesrs863223646
hgdprs863223646
ensemblrs863223646
gopubmedrs863223646
geneviewrs863223646
scholarrs863223646
googlers863223646
pharmgkbrs863223646
gwascentralrs863223646
openSNPrs863223646
23andMers863223646
23andMe allrs863223646
SNP Nexus

SNPshotrs863223646
SNPdbers863223646
MSV3drs863223646
GWAS Ctlgrs863223646
Max Magnitude0
ClinVar
Risk rs863223646(-;-)
Alt rs863223646(-;-)
Reference Rs863223646(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153580717delG
CLNSRC
CLNACC RCV000199101.2,