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rs1064797332

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome6
Position152395671
GeneSYNE1
is asnp
is mentioned by
dbSNPrs1064797332
dbSNP (classic)rs1064797332
ClinGenrs1064797332
ebirs1064797332
HLIrs1064797332
Exacrs1064797332
Gnomadrs1064797332
Varsomers1064797332
LitVarrs1064797332
Maprs1064797332
PheGenIrs1064797332
Biobankrs1064797332
1000 genomesrs1064797332
hgdprs1064797332
ensemblrs1064797332
geneviewrs1064797332
scholarrs1064797332
googlers1064797332
pharmgkbrs1064797332
gwascentralrs1064797332
openSNPrs1064797332
23andMers1064797332
23andMe allrs1064797332
SNPshotrs1064797332
SNPdbers1064797332
MSV3drs1064797332
GWAS Ctlgrs1064797332
Max Magnitude0
ClinVar
Risk rs1064797332(-;-)
Alt rs1064797332(-;-)
Reference Rs1064797332(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SYNE1
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.152716806delG
CLNSRC
CLNACC RCV000487909.1,