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rs786205194

From SNPedia

Orientationminus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs786205194(-;-)
Make rs786205194(-;GC)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154358336
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205194
ebirs786205194
HLIrs786205194
Exacrs786205194
Varsomers786205194
Maprs786205194
PheGenIrs786205194
hapmaprs786205194
1000 genomesrs786205194
hgdprs786205194
ensemblrs786205194
gopubmedrs786205194
geneviewrs786205194
scholarrs786205194
googlers786205194
pharmgkbrs786205194
gwascentralrs786205194
openSNPrs786205194
23andMers786205194
23andMe allrs786205194
SNP Nexus

SNPshotrs786205194
SNPdbers786205194
MSV3drs786205194
GWAS Ctlgrs786205194
Max Magnitude0
ClinVar
Risk rs786205194(;)
Alt rs786205194(;)
Reference rs786205194(GC;GC)
Significance Probable-Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153586704_153586705delGC
CLNSRC Claritas Genomics
CLNACC RCV000170416.1,