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rs370490152

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs370490152(C;T)
Make rs370490152(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position154366582
GeneFLNA
is asnp
is mentioned by
dbSNPrs370490152
ebirs370490152
HLIrs370490152
Exacrs370490152
Varsomers370490152
Maprs370490152
PheGenIrs370490152
hapmaprs370490152
1000 genomesrs370490152
hgdprs370490152
ensemblrs370490152
gopubmedrs370490152
geneviewrs370490152
scholarrs370490152
googlers370490152
pharmgkbrs370490152
gwascentralrs370490152
openSNPrs370490152
23andMers370490152
23andMe allrs370490152
SNP Nexus

SNPshotrs370490152
SNPdbers370490152
MSV3drs370490152
GWAS Ctlgrs370490152
Max Magnitude0
ClinVar
Risk rs370490152(T;T)
Alt rs370490152(T;T)
Reference rs370490152(C;C)
Significance Probable-Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 0
HGVS NC_000023.10:g.153594950C>A
CLNSRC Claritas Genomics
CLNACC RCV000170399.1,