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rs1060499769

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499769(A;A)
Make rs1060499769(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position152354858
GeneSYNE1
is asnp
is mentioned by
dbSNPrs1060499769
dbSNP (old)rs1060499769
ClinGenrs1060499769
ebirs1060499769
HLIrs1060499769
Exacrs1060499769
Gnomadrs1060499769
Varsomers1060499769
Maprs1060499769
PheGenIrs1060499769
Biobankrs1060499769
1000 genomesrs1060499769
hgdprs1060499769
ensemblrs1060499769
gopubmedrs1060499769
geneviewrs1060499769
scholarrs1060499769
googlers1060499769
pharmgkbrs1060499769
gwascentralrs1060499769
openSNPrs1060499769
23andMers1060499769
23andMe allrs1060499769
SNPshotrs1060499769
SNPdbers1060499769
MSV3drs1060499769
GWAS Ctlgrs1060499769
Max Magnitude0
ClinVar
Risk rs1060499769(A;A)
Alt rs1060499769(A;A)
Reference Rs1060499769(G;G)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene SYNE1
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000006.11:g.152675993C>T
CLNSRC
CLNACC RCV000454183.1,