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rs1064794589

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome19
Position35032595
GeneSCN1B
is asnp
is mentioned by
dbSNPrs1064794589
dbSNP (old)rs1064794589
ClinGenrs1064794589
ebirs1064794589
HLIrs1064794589
Exacrs1064794589
Gnomadrs1064794589
Varsomers1064794589
LitVarrs1064794589
Maprs1064794589
PheGenIrs1064794589
Biobankrs1064794589
1000 genomesrs1064794589
hgdprs1064794589
ensemblrs1064794589
gopubmedrs1064794589
geneviewrs1064794589
scholarrs1064794589
googlers1064794589
pharmgkbrs1064794589
gwascentralrs1064794589
openSNPrs1064794589
23andMers1064794589
23andMe allrs1064794589
SNPshotrs1064794589
SNPdbers1064794589
MSV3drs1064794589
GWAS Ctlgrs1064794589
Max Magnitude0
ClinVar
Risk rs1064794589(-;-)
Alt rs1064794589(-;-)
Reference Rs1064794589(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1B
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.35523499delC
CLNSRC
CLNACC RCV000480433.1,