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rs863223645

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223645(-;C)
Make rs863223645(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154360386
GeneFLNA
is asnp
is mentioned by
dbSNPrs863223645
ClinGenrs863223645
ebirs863223645
HLIrs863223645
Exacrs863223645
Varsomers863223645
Maprs863223645
PheGenIrs863223645
hapmaprs863223645
1000 genomesrs863223645
hgdprs863223645
ensemblrs863223645
gopubmedrs863223645
geneviewrs863223645
scholarrs863223645
googlers863223645
pharmgkbrs863223645
gwascentralrs863223645
openSNPrs863223645
23andMers863223645
23andMe allrs863223645
SNP Nexus

SNPshotrs863223645
SNPdbers863223645
MSV3drs863223645
GWAS Ctlgrs863223645
Max Magnitude0
ClinVar
Risk rs863223645(C;C)
Alt rs863223645(C;C)
Reference Rs863223645(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153588755dupG
CLNSRC
CLNACC RCV000196857.1,