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rs1057521251

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521251(G;T)
Make rs1057521251(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position153592547
GeneFAM58A
is asnp
is mentioned by
dbSNPrs1057521251
dbSNP (old)rs1057521251
ClinGenrs1057521251
ebirs1057521251
HLIrs1057521251
Exacrs1057521251
Gnomadrs1057521251
Varsomers1057521251
Maprs1057521251
PheGenIrs1057521251
Biobankrs1057521251
1000 genomesrs1057521251
hgdprs1057521251
ensemblrs1057521251
gopubmedrs1057521251
geneviewrs1057521251
scholarrs1057521251
googlers1057521251
pharmgkbrs1057521251
gwascentralrs1057521251
openSNPrs1057521251
23andMers1057521251
23andMe allrs1057521251
SNPshotrs1057521251
SNPdbers1057521251
MSV3drs1057521251
GWAS Ctlgrs1057521251
Max Magnitude0
ClinVar
Risk rs1057521251(T;T)
Alt rs1057521251(T;T)
Reference Rs1057521251(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FAM58A
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.152858005C>A
CLNSRC
CLNACC RCV000434465.1,