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rs786205179

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205179(G;T)
Make rs786205179(T;T)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154366582
is asnp
is mentioned by
dbSNPrs786205179
ebirs786205179
HLIrs786205179
Exacrs786205179
Varsomers786205179
Maprs786205179
PheGenIrs786205179
hapmaprs786205179
1000 genomesrs786205179
hgdprs786205179
ensemblrs786205179
gopubmedrs786205179
geneviewrs786205179
scholarrs786205179
googlers786205179
pharmgkbrs786205179
gwascentralrs786205179
openSNPrs786205179
23andMers786205179
23andMe allrs786205179
SNP Nexus

SNPshotrs786205179
SNPdbers786205179
MSV3drs786205179
GWAS Ctlgrs786205179
Max Magnitude0
ClinVar
Risk rs786205179(T;T)
Alt rs786205179(T;T)
Reference rs786205179(G;G)
Significance Probable-Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153594950C>A
CLNSRC Claritas Genomics
CLNACC RCV000170399.1,