Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057521813

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521813(G;G)
Make rs1057521813(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position152385791
GeneSYNE1
is asnp
is mentioned by
dbSNPrs1057521813
dbSNP (classic)rs1057521813
ClinGenrs1057521813
ebirs1057521813
HLIrs1057521813
Exacrs1057521813
Gnomadrs1057521813
Varsomers1057521813
LitVarrs1057521813
Maprs1057521813
PheGenIrs1057521813
Biobankrs1057521813
1000 genomesrs1057521813
hgdprs1057521813
ensemblrs1057521813
geneviewrs1057521813
scholarrs1057521813
googlers1057521813
pharmgkbrs1057521813
gwascentralrs1057521813
openSNPrs1057521813
23andMers1057521813
23andMe allrs1057521813
SNPshotrs1057521813
SNPdbers1057521813
MSV3drs1057521813
GWAS Ctlgrs1057521813
Max Magnitude0
ClinVar
Risk rs1057521813(G;G)
Alt rs1057521813(G;G)
Reference Rs1057521813(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SYNE1
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.152706926A>C
CLNSRC
CLNACC RCV000428337.1,