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rs1057518202

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518202(-;AAAT)
Make rs1057518202(AAAT;AAAT)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position80704797
GeneBRWD3
is asnp
is mentioned by
dbSNPrs1057518202
dbSNP (old)rs1057518202
ClinGenrs1057518202
ebirs1057518202
HLIrs1057518202
Exacrs1057518202
Gnomadrs1057518202
Varsomers1057518202
Maprs1057518202
PheGenIrs1057518202
Biobankrs1057518202
1000 genomesrs1057518202
hgdprs1057518202
ensemblrs1057518202
gopubmedrs1057518202
geneviewrs1057518202
scholarrs1057518202
googlers1057518202
pharmgkbrs1057518202
gwascentralrs1057518202
openSNPrs1057518202
23andMers1057518202
23andMe allrs1057518202
SNPshotrs1057518202
SNPdbers1057518202
MSV3drs1057518202
GWAS Ctlgrs1057518202
Max Magnitude0
ClinVar
Risk rs1057518202(AAAT;AAAT)
Alt rs1057518202(AAAT;AAAT)
Reference Rs1057518202(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene BRWD3
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.79960297_79960300dupATTT
CLNSRC
CLNACC RCV000413023.1,