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rs1057518603

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518603(-;-)
Make rs1057518603(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position152323498
GeneSYNE1
is asnp
is mentioned by
dbSNPrs1057518603
dbSNP (classic)rs1057518603
ClinGenrs1057518603
ebirs1057518603
HLIrs1057518603
Exacrs1057518603
Gnomadrs1057518603
Varsomers1057518603
LitVarrs1057518603
Maprs1057518603
PheGenIrs1057518603
Biobankrs1057518603
1000 genomesrs1057518603
hgdprs1057518603
ensemblrs1057518603
geneviewrs1057518603
scholarrs1057518603
googlers1057518603
pharmgkbrs1057518603
gwascentralrs1057518603
openSNPrs1057518603
23andMers1057518603
SNPshotrs1057518603
SNPdbers1057518603
MSV3drs1057518603
GWAS Ctlgrs1057518603
Max Magnitude0
ClinVar
Risk rs1057518603(-;-)
Alt rs1057518603(-;-)
Reference Rs1057518603(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SYNE1
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.152644633delG
CLNSRC
CLNACC RCV000414261.1,