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rs781910090

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs781910090(A;A)
Make rs781910090(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154351689
GeneFLNA
is asnp
is mentioned by
dbSNPrs781910090
ebirs781910090
HLIrs781910090
Exacrs781910090
Varsomers781910090
Maprs781910090
PheGenIrs781910090
hapmaprs781910090
1000 genomesrs781910090
hgdprs781910090
ensemblrs781910090
gopubmedrs781910090
geneviewrs781910090
scholarrs781910090
googlers781910090
pharmgkbrs781910090
gwascentralrs781910090
openSNPrs781910090
23andMers781910090
23andMe allrs781910090
SNP Nexus

SNPshotrs781910090
SNPdbers781910090
MSV3drs781910090
GWAS Ctlgrs781910090
Max Magnitude0
ClinVar
Risk rs781910090(A;A)
Alt rs781910090(A;A)
Reference rs781910090(G;G)
Significance Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 0
HGVS NC_000023.10:g.153580057G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012519.23,