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rs786205186

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205186(C;C)
Make rs786205186(C;G)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154362417
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205186
ebirs786205186
HLIrs786205186
Exacrs786205186
Varsomers786205186
Maprs786205186
PheGenIrs786205186
hapmaprs786205186
1000 genomesrs786205186
hgdprs786205186
ensemblrs786205186
gopubmedrs786205186
geneviewrs786205186
scholarrs786205186
googlers786205186
pharmgkbrs786205186
gwascentralrs786205186
openSNPrs786205186
23andMers786205186
23andMe allrs786205186
SNP Nexus

SNPshotrs786205186
SNPdbers786205186
MSV3drs786205186
GWAS Ctlgrs786205186
Max Magnitude0
ClinVar
Risk rs786205186(C;C)
Alt rs786205186(C;C)
Reference rs786205186(G;G)
Significance Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153590785C>G
CLNSRC
CLNACC RCV000170407.1,