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rs786205203

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205203(-;-)
Make rs786205203(-;C)
Make rs786205203(C;C)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154367532
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205203
ebirs786205203
HLIrs786205203
Exacrs786205203
Varsomers786205203
Maprs786205203
PheGenIrs786205203
hapmaprs786205203
1000 genomesrs786205203
hgdprs786205203
ensemblrs786205203
gopubmedrs786205203
geneviewrs786205203
scholarrs786205203
googlers786205203
pharmgkbrs786205203
gwascentralrs786205203
openSNPrs786205203
23andMers786205203
23andMe allrs786205203
SNP Nexus

SNPshotrs786205203
SNPdbers786205203
MSV3drs786205203
GWAS Ctlgrs786205203
Max Magnitude0
ClinVar
Risk rs786205203(C;C)
Alt rs786205203(C;C)
Reference rs786205203(;)
Significance Probable-Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153595901dupG
CLNSRC
CLNACC RCV000170425.1,