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rs1064795360

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position128219208
GeneDNM1
is asnp
is mentioned by
dbSNPrs1064795360
dbSNP (classic)rs1064795360
ClinGenrs1064795360
ebirs1064795360
HLIrs1064795360
Exacrs1064795360
Gnomadrs1064795360
Varsomers1064795360
LitVarrs1064795360
Maprs1064795360
PheGenIrs1064795360
Biobankrs1064795360
1000 genomesrs1064795360
hgdprs1064795360
ensemblrs1064795360
geneviewrs1064795360
scholarrs1064795360
googlers1064795360
pharmgkbrs1064795360
gwascentralrs1064795360
openSNPrs1064795360
23andMers1064795360
SNPshotrs1064795360
SNPdbers1064795360
MSV3drs1064795360
GWAS Ctlgrs1064795360
Max Magnitude0
ClinVar
Risk rs1064795360(A;A)
Alt rs1064795360(A;A)
Reference Rs1064795360(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DNM1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130981487C>A
CLNSRC
CLNACC RCV000483428.1,