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rs1057518038

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518038(A;G)
Make rs1057518038(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position147940643
GeneFMR1
is asnp
is mentioned by
dbSNPrs1057518038
dbSNP (old)rs1057518038
ClinGenrs1057518038
ebirs1057518038
HLIrs1057518038
Exacrs1057518038
Gnomadrs1057518038
Varsomers1057518038
Maprs1057518038
PheGenIrs1057518038
Biobankrs1057518038
1000 genomesrs1057518038
hgdprs1057518038
ensemblrs1057518038
gopubmedrs1057518038
geneviewrs1057518038
scholarrs1057518038
googlers1057518038
pharmgkbrs1057518038
gwascentralrs1057518038
openSNPrs1057518038
23andMers1057518038
23andMe allrs1057518038
SNPshotrs1057518038
SNPdbers1057518038
MSV3drs1057518038
GWAS Ctlgrs1057518038
Max Magnitude0
ClinVar
Risk rs1057518038(G;G)
Alt rs1057518038(G;G)
Reference Rs1057518038(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FMR1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.147022162A>G
CLNSRC
CLNACC RCV000413972.1,