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rs863223635

From SNPedia

Orientationminus
Make rs863223635(-;-)
Make rs863223635(-;GGG)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154348893
GeneFLNA
is asnp
is mentioned by
dbSNPrs863223635
ebirs863223635
HLIrs863223635
Exacrs863223635
Varsomers863223635
Maprs863223635
PheGenIrs863223635
hapmaprs863223635
1000 genomesrs863223635
hgdprs863223635
ensemblrs863223635
gopubmedrs863223635
geneviewrs863223635
scholarrs863223635
googlers863223635
pharmgkbrs863223635
gwascentralrs863223635
openSNPrs863223635
23andMers863223635
23andMe allrs863223635
SNP Nexus

SNPshotrs863223635
SNPdbers863223635
MSV3drs863223635
GWAS Ctlgrs863223635
Max Magnitude
ClinVar
Risk rs863223635(;)
Alt rs863223635(;)
Reference rs863223635(GGG;GGG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153577261_153577263delCCC
CLNSRC
CLNACC RCV000196351.1,