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rs137853315

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853315(C;T)
Make rs137853315(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154368081
GeneFLNA
is asnp
is mentioned by
dbSNPrs137853315
ebirs137853315
HLIrs137853315
Exacrs137853315
Varsomers137853315
Maprs137853315
PheGenIrs137853315
hapmaprs137853315
1000 genomesrs137853315
hgdprs137853315
ensemblrs137853315
gopubmedrs137853315
geneviewrs137853315
scholarrs137853315
googlers137853315
pharmgkbrs137853315
gwascentralrs137853315
openSNPrs137853315
23andMers137853315
23andMe allrs137853315
SNP Nexus

SNPshotrs137853315
SNPdbers137853315
MSV3drs137853315
GWAS Ctlgrs137853315
Max Magnitude0
OMIM300017
Desc
Variant0021
Relatedalso
ClinVar
Risk rs137853315(T;T)
Alt rs137853315(T;T)
Reference rs137853315(C;C)
Significance Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153596449G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012533.14,