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rs863223634

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223634(-;C)
Make rs863223634(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154352667
GeneFLNA
is asnp
is mentioned by
dbSNPrs863223634
ClinGenrs863223634
ebirs863223634
HLIrs863223634
Exacrs863223634
Varsomers863223634
Maprs863223634
PheGenIrs863223634
hapmaprs863223634
1000 genomesrs863223634
hgdprs863223634
ensemblrs863223634
gopubmedrs863223634
geneviewrs863223634
scholarrs863223634
googlers863223634
pharmgkbrs863223634
gwascentralrs863223634
openSNPrs863223634
23andMers863223634
23andMe allrs863223634
SNP Nexus

SNPshotrs863223634
SNPdbers863223634
MSV3drs863223634
GWAS Ctlgrs863223634
Max Magnitude0
ClinVar
Risk rs863223634(C;C)
Alt rs863223634(C;C)
Reference Rs863223634(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153581036dupG
CLNSRC
CLNACC RCV000198038.1,