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

rs1057520134

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520134(C;G)
Make rs1057520134(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position152239701
GeneSYNE1
is asnp
is mentioned by
dbSNPrs1057520134
dbSNP (old)rs1057520134
ClinGenrs1057520134
ebirs1057520134
HLIrs1057520134
Exacrs1057520134
Gnomadrs1057520134
Varsomers1057520134
Maprs1057520134
PheGenIrs1057520134
Biobankrs1057520134
1000 genomesrs1057520134
hgdprs1057520134
ensemblrs1057520134
gopubmedrs1057520134
geneviewrs1057520134
scholarrs1057520134
googlers1057520134
pharmgkbrs1057520134
gwascentralrs1057520134
openSNPrs1057520134
23andMers1057520134
23andMe allrs1057520134
SNPshotrs1057520134
SNPdbers1057520134
MSV3drs1057520134
GWAS Ctlgrs1057520134
Max Magnitude0
ClinVar
Risk rs1057520134(G;G)
Alt rs1057520134(G;G)
Reference Rs1057520134(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SYNE1
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.152560836G>C
CLNSRC
CLNACC RCV000445042.1,