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rs863223633

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223633(-;GGTG)
Make rs863223633(GGTG;GGTG)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154359551
GeneFLNA
is asnp
is mentioned by
dbSNPrs863223633
ClinGenrs863223633
ebirs863223633
HLIrs863223633
Exacrs863223633
Varsomers863223633
Maprs863223633
PheGenIrs863223633
hapmaprs863223633
1000 genomesrs863223633
hgdprs863223633
ensemblrs863223633
gopubmedrs863223633
geneviewrs863223633
scholarrs863223633
googlers863223633
pharmgkbrs863223633
gwascentralrs863223633
openSNPrs863223633
23andMers863223633
23andMe allrs863223633
SNP Nexus

SNPshotrs863223633
SNPdbers863223633
MSV3drs863223633
GWAS Ctlgrs863223633
Max Magnitude0
ClinVar
Risk rs863223633(GGTG;GGTG)
Alt rs863223633(GGTG;GGTG)
Reference Rs863223633(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153587920_153587923dupCACC
CLNSRC
CLNACC RCV000196372.1,