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rs1064797369

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position47572956
GeneSYN1
is asnp
is mentioned by
dbSNPrs1064797369
dbSNP (old)rs1064797369
ClinGenrs1064797369
ebirs1064797369
HLIrs1064797369
Exacrs1064797369
Gnomadrs1064797369
Varsomers1064797369
Maprs1064797369
PheGenIrs1064797369
Biobankrs1064797369
1000 genomesrs1064797369
hgdprs1064797369
ensemblrs1064797369
gopubmedrs1064797369
geneviewrs1064797369
scholarrs1064797369
googlers1064797369
pharmgkbrs1064797369
gwascentralrs1064797369
openSNPrs1064797369
23andMers1064797369
23andMe allrs1064797369
SNPshotrs1064797369
SNPdbers1064797369
MSV3drs1064797369
GWAS Ctlgrs1064797369
Max Magnitude0
ClinVar
Risk rs1064797369(-;-)
Alt rs1064797369(-;-)
Reference Rs1064797369(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SYN1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.47432355delC
CLNSRC
CLNACC RCV000487970.1,