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rs398123622

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398123622(C;G)
Make rs398123622(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154367741
GeneFLNA
is asnp
is mentioned by
dbSNPrs398123622
ebirs398123622
HLIrs398123622
Exacrs398123622
Varsomers398123622
Maprs398123622
PheGenIrs398123622
hapmaprs398123622
1000 genomesrs398123622
hgdprs398123622
ensemblrs398123622
gopubmedrs398123622
geneviewrs398123622
scholarrs398123622
googlers398123622
pharmgkbrs398123622
gwascentralrs398123622
openSNPrs398123622
23andMers398123622
23andMe allrs398123622
SNP Nexus

SNPshotrs398123622
SNPdbers398123622
MSV3drs398123622
GWAS Ctlgrs398123622
Max Magnitude0
ClinVar
Risk rs398123622(G;G)
Alt rs398123622(G;G)
Reference rs398123622(C;C)
Significance Pathogenic
Disease X-linked periventricular heterotopia not provided
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia not provided
Reversed 1
HGVS NC_000023.10:g.153596109G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012515.22, RCV000079706.4,