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rs786205183

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205183(A;G)
Make rs786205183(G;G)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154364721
GeneFLNA
is asnp
is mentioned by
dbSNPrs786205183
ebirs786205183
HLIrs786205183
Exacrs786205183
Varsomers786205183
Maprs786205183
PheGenIrs786205183
hapmaprs786205183
1000 genomesrs786205183
hgdprs786205183
ensemblrs786205183
gopubmedrs786205183
geneviewrs786205183
scholarrs786205183
googlers786205183
pharmgkbrs786205183
gwascentralrs786205183
openSNPrs786205183
23andMers786205183
23andMe allrs786205183
SNP Nexus

SNPshotrs786205183
SNPdbers786205183
MSV3drs786205183
GWAS Ctlgrs786205183
Max Magnitude0
ClinVar
Risk rs786205183(G;G)
Alt rs786205183(G;G)
Reference rs786205183(A;A)
Significance Pathogenic
Disease X-linked periventricular heterotopia
Variation info
Gene FLNA
CLNDBN X-linked periventricular heterotopia
Reversed 1
HGVS NC_000023.10:g.153593089T>C
CLNSRC
CLNACC RCV000170404.1,