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rs786205198

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205198(-;-)
Make rs786205198(-;C)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154357436
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205198
ebirs786205198
HLIrs786205198
Exacrs786205198
Varsomers786205198
Maprs786205198
PheGenIrs786205198
hapmaprs786205198
1000 genomesrs786205198
hgdprs786205198
ensemblrs786205198
gopubmedrs786205198
geneviewrs786205198
scholarrs786205198
googlers786205198
pharmgkbrs786205198
gwascentralrs786205198
openSNPrs786205198
23andMers786205198
23andMe allrs786205198
SNP Nexus

SNPshotrs786205198
SNPdbers786205198
MSV3drs786205198
GWAS Ctlgrs786205198
Max Magnitude0
ClinVar
Risk rs786205198(;)
Alt rs786205198(;)
Reference rs786205198(C;C)
Significance Probable-Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153585804delG
CLNSRC Claritas Genomics
CLNACC RCV000170420.1,