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rs1057517938

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517938(C;T)
Make rs1057517938(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position143922290
GenePLEC
is asnp
is mentioned by
dbSNPrs1057517938
dbSNP (old)rs1057517938
ClinGenrs1057517938
ebirs1057517938
HLIrs1057517938
Exacrs1057517938
Gnomadrs1057517938
Varsomers1057517938
Maprs1057517938
PheGenIrs1057517938
Biobankrs1057517938
1000 genomesrs1057517938
hgdprs1057517938
ensemblrs1057517938
gopubmedrs1057517938
geneviewrs1057517938
scholarrs1057517938
googlers1057517938
pharmgkbrs1057517938
gwascentralrs1057517938
openSNPrs1057517938
23andMers1057517938
23andMe allrs1057517938
SNPshotrs1057517938
SNPdbers1057517938
MSV3drs1057517938
GWAS Ctlgrs1057517938
Max Magnitude0
ClinVar
Risk rs1057517938(T;T)
Alt rs1057517938(T;T)
Reference Rs1057517938(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PLEC
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.144996458G>A
CLNSRC
CLNACC RCV000414097.1,