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rs587783629

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587783629(-;-)
Make rs587783629(-;CC)
Make rs587783629(CC;CC)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position28767415
GeneFOXG1
is asnp
is mentioned by
dbSNPrs587783629
ebirs587783629
HLIrs587783629
Exacrs587783629
Varsomers587783629
Maprs587783629
PheGenIrs587783629
hapmaprs587783629
1000 genomesrs587783629
hgdprs587783629
ensemblrs587783629
gopubmedrs587783629
geneviewrs587783629
scholarrs587783629
googlers587783629
pharmgkbrs587783629
gwascentralrs587783629
openSNPrs587783629
23andMers587783629
23andMe allrs587783629
SNP Nexus

SNPshotrs587783629
SNPdbers587783629
MSV3drs587783629
GWAS Ctlgrs587783629
Max Magnitude0
ClinVar
Risk rs587783629(AC,ACC;AC,ACC)
Alt rs587783629(AC,ACC;AC,ACC)
Reference rs587783629(A;A)
Significance Pathogenic
Disease Rett syndrome not provided
Variation info
Gene FOXG1
CLNDBN Rett syndrome, congenital variant not provided
Reversed 0
HGVS NC_000014.8:g.29236620_29236621dupCC; NC_000014.8:g.29236621dupC
CLNSRC
CLNACC RCV000145981.1, RCV000187470.1,