Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057519155

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519155(-;-)
Make rs1057519155(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position143924876
GenePLEC
is asnp
is mentioned by
dbSNPrs1057519155
dbSNP (old)rs1057519155
ClinGenrs1057519155
ebirs1057519155
HLIrs1057519155
Exacrs1057519155
Gnomadrs1057519155
Varsomers1057519155
Maprs1057519155
PheGenIrs1057519155
Biobankrs1057519155
1000 genomesrs1057519155
hgdprs1057519155
ensemblrs1057519155
gopubmedrs1057519155
geneviewrs1057519155
scholarrs1057519155
googlers1057519155
pharmgkbrs1057519155
gwascentralrs1057519155
openSNPrs1057519155
23andMers1057519155
23andMe allrs1057519155
SNPshotrs1057519155
SNPdbers1057519155
MSV3drs1057519155
GWAS Ctlgrs1057519155
Max Magnitude0
ClinVar
Risk rs1057519155(-;-)
Alt rs1057519155(-;-)
Reference Rs1057519155(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PLEC
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.144999044delG
CLNSRC
CLNACC RCV000416203.1,