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rs863223636

From SNPedia

Orientationminus
Make rs863223636(-;-)
Make rs863223636(-;CT)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154348851
GeneFLNA
is asnp
is mentioned by
dbSNPrs863223636
ebirs863223636
HLIrs863223636
Exacrs863223636
Varsomers863223636
Maprs863223636
PheGenIrs863223636
hapmaprs863223636
1000 genomesrs863223636
hgdprs863223636
ensemblrs863223636
gopubmedrs863223636
geneviewrs863223636
scholarrs863223636
googlers863223636
pharmgkbrs863223636
gwascentralrs863223636
openSNPrs863223636
23andMers863223636
23andMe allrs863223636
SNP Nexus

SNPshotrs863223636
SNPdbers863223636
MSV3drs863223636
GWAS Ctlgrs863223636
Max Magnitude
ClinVar
Risk rs863223636(;)
Alt rs863223636(;)
Reference rs863223636(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene FLNA
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153577219_153577220delAG
CLNSRC
CLNACC RCV000198493.1,