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rs1057518850

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518850(A;G)
Make rs1057518850(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position147928320
GeneFMR1
is asnp
is mentioned by
dbSNPrs1057518850
dbSNP (old)rs1057518850
ClinGenrs1057518850
ebirs1057518850
HLIrs1057518850
Exacrs1057518850
Gnomadrs1057518850
Varsomers1057518850
Maprs1057518850
PheGenIrs1057518850
Biobankrs1057518850
1000 genomesrs1057518850
hgdprs1057518850
ensemblrs1057518850
gopubmedrs1057518850
geneviewrs1057518850
scholarrs1057518850
googlers1057518850
pharmgkbrs1057518850
gwascentralrs1057518850
openSNPrs1057518850
23andMers1057518850
23andMe allrs1057518850
SNPshotrs1057518850
SNPdbers1057518850
MSV3drs1057518850
GWAS Ctlgrs1057518850
Max Magnitude0
ClinVar
Risk rs1057518850(G;G)
Alt rs1057518850(G;G)
Reference Rs1057518850(A;A)
Significance Probable-Pathogenic
Disease Autistic behavior Intellectual disability
Variation info
Gene FMR1
CLNDBN Autistic behavior Intellectual disability
Reversed 0
HGVS NC_000023.10:g.147009838A>G
CLNSRC
CLNACC RCV000415417.1,