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rs1064797188

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome14
Position64003330
GeneSYNE2
is asnp
is mentioned by
dbSNPrs1064797188
dbSNP (old)rs1064797188
ClinGenrs1064797188
ebirs1064797188
HLIrs1064797188
Exacrs1064797188
Gnomadrs1064797188
Varsomers1064797188
Maprs1064797188
PheGenIrs1064797188
Biobankrs1064797188
1000 genomesrs1064797188
hgdprs1064797188
ensemblrs1064797188
gopubmedrs1064797188
geneviewrs1064797188
scholarrs1064797188
googlers1064797188
pharmgkbrs1064797188
gwascentralrs1064797188
openSNPrs1064797188
23andMers1064797188
23andMe allrs1064797188
SNPshotrs1064797188
SNPdbers1064797188
MSV3drs1064797188
GWAS Ctlgrs1064797188
Max Magnitude0
ClinVar
Risk rs1064797188(A;A)
Alt rs1064797188(A;A)
Reference Rs1064797188(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SYNE2
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.64470048G>A
CLNSRC
CLNACC RCV000488136.1,