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rs137853311

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853311(C;T)
Make rs137853311(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154364582
GeneFLNA
is asnp
is mentioned by
dbSNPrs137853311
ebirs137853311
HLIrs137853311
Exacrs137853311
Varsomers137853311
Maprs137853311
PheGenIrs137853311
hapmaprs137853311
1000 genomesrs137853311
hgdprs137853311
ensemblrs137853311
gopubmedrs137853311
geneviewrs137853311
scholarrs137853311
googlers137853311
pharmgkbrs137853311
gwascentralrs137853311
openSNPrs137853311
23andMers137853311
23andMe allrs137853311
SNP Nexus

SNPshotrs137853311
SNPdbers137853311
MSV3drs137853311
GWAS Ctlgrs137853311
Max Magnitude0
OMIM300017
Desc
Variant0006
Relatedalso
ClinVar
Risk rs137853311(T;T)
Alt rs137853311(T;T)
Reference rs137853311(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.153592950G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012518.22,