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rs863223628

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223628(A;C)
Make rs863223628(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154367955
GeneFLNA
is asnp
is mentioned by
dbSNPrs863223628
ebirs863223628
HLIrs863223628
Exacrs863223628
Varsomers863223628
Maprs863223628
PheGenIrs863223628
hapmaprs863223628
1000 genomesrs863223628
hgdprs863223628
ensemblrs863223628
gopubmedrs863223628
geneviewrs863223628
scholarrs863223628
googlers863223628
pharmgkbrs863223628
gwascentralrs863223628
openSNPrs863223628
23andMers863223628
23andMe allrs863223628
SNP Nexus

SNPshotrs863223628
SNPdbers863223628
MSV3drs863223628
GWAS Ctlgrs863223628
Max Magnitude0
ClinVar
Risk rs863223628(C;C)
Alt rs863223628(C;C)
Reference Rs863223628(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153596323T>G
CLNSRC UniProtKB (protein)
CLNACC RCV000199318.1,