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rs863223297

From SNPedia

Orientationminus
Make rs863223297(-;-)
Make rs863223297(-;GGCCC)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154370955
GeneFLNA
is asnp
is mentioned by
dbSNPrs863223297
ebirs863223297
HLIrs863223297
Exacrs863223297
Varsomers863223297
Maprs863223297
PheGenIrs863223297
hapmaprs863223297
1000 genomesrs863223297
hgdprs863223297
ensemblrs863223297
gopubmedrs863223297
geneviewrs863223297
scholarrs863223297
googlers863223297
pharmgkbrs863223297
gwascentralrs863223297
openSNPrs863223297
23andMers863223297
23andMe allrs863223297
SNP Nexus

SNPshotrs863223297
SNPdbers863223297
MSV3drs863223297
GWAS Ctlgrs863223297
Max Magnitude
ClinVar
Risk rs863223297(;)
Alt rs863223297(;)
Reference rs863223297(GGCCC;GGCCC)
Significance Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153599323_153599327delGGGCC
CLNSRC OMIM Allelic Variant
CLNACC RCV000012517.16,