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rs786205190

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205190(-;-)
Make rs786205190(-;TCCAGGACTGCACTCC)
Make rs786205190(TCCAGGACTGCACTCC;TCCAGGACTGCACTCC)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154359635
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205190
ebirs786205190
HLIrs786205190
Exacrs786205190
Varsomers786205190
Maprs786205190
PheGenIrs786205190
hapmaprs786205190
1000 genomesrs786205190
hgdprs786205190
ensemblrs786205190
gopubmedrs786205190
geneviewrs786205190
scholarrs786205190
googlers786205190
pharmgkbrs786205190
gwascentralrs786205190
openSNPrs786205190
23andMers786205190
23andMe allrs786205190
SNP Nexus

SNPshotrs786205190
SNPdbers786205190
MSV3drs786205190
GWAS Ctlgrs786205190
Max Magnitude0
ClinVar
Risk rs786205190(TCCAGGACTGCACTCC;TCCAGGACTGCACTCC)
Alt rs786205190(TCCAGGACTGCACTCC;TCCAGGACTGCACTCC)
Reference rs786205190(;)
Significance Probable-Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153588004_153588019dup16
CLNSRC Claritas Genomics
CLNACC RCV000170411.1,