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rs863223641

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223641(A;A)
Make rs863223641(A;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154367964
GeneFLNA
is asnp
is mentioned by
dbSNPrs863223641
ebirs863223641
HLIrs863223641
Exacrs863223641
Varsomers863223641
Maprs863223641
PheGenIrs863223641
hapmaprs863223641
1000 genomesrs863223641
hgdprs863223641
ensemblrs863223641
gopubmedrs863223641
geneviewrs863223641
scholarrs863223641
googlers863223641
pharmgkbrs863223641
gwascentralrs863223641
openSNPrs863223641
23andMers863223641
23andMe allrs863223641
SNP Nexus

SNPshotrs863223641
SNPdbers863223641
MSV3drs863223641
GWAS Ctlgrs863223641
Max Magnitude0
ClinVar
Risk rs863223641(A;A)
Alt rs863223641(A;A)
Reference rs863223641(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153596332G>T
CLNSRC
CLNACC RCV000196613.1,