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rs786205488

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205488(C;T)
Make rs786205488(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position64007107
GeneSYNE2
is asnp
is mentioned by
dbSNPrs786205488
ebirs786205488
HLIrs786205488
Exacrs786205488
Varsomers786205488
Maprs786205488
PheGenIrs786205488
hapmaprs786205488
1000 genomesrs786205488
hgdprs786205488
ensemblrs786205488
gopubmedrs786205488
geneviewrs786205488
scholarrs786205488
googlers786205488
pharmgkbrs786205488
gwascentralrs786205488
openSNPrs786205488
23andMers786205488
23andMe allrs786205488
SNP Nexus

SNPshotrs786205488
SNPdbers786205488
MSV3drs786205488
GWAS Ctlgrs786205488
Max Magnitude0
ClinVar
Risk rs786205488(T;T)
Alt rs786205488(T;T)
Reference rs786205488(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SYNE2
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.64473825C>T
CLNSRC
CLNACC RCV000171223.1,