Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064793101

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome19
Position10793797
GeneDNM2
is asnp
is mentioned by
dbSNPrs1064793101
dbSNP (classic)rs1064793101
ClinGenrs1064793101
ebirs1064793101
HLIrs1064793101
Exacrs1064793101
Gnomadrs1064793101
Varsomers1064793101
LitVarrs1064793101
Maprs1064793101
PheGenIrs1064793101
Biobankrs1064793101
1000 genomesrs1064793101
hgdprs1064793101
ensemblrs1064793101
geneviewrs1064793101
scholarrs1064793101
googlers1064793101
pharmgkbrs1064793101
gwascentralrs1064793101
openSNPrs1064793101
23andMers1064793101
23andMe allrs1064793101
SNPshotrs1064793101
SNPdbers1064793101
MSV3drs1064793101
GWAS Ctlgrs1064793101
Max Magnitude0
ClinVar
Risk rs1064793101(T;T)
Alt rs1064793101(T;T)
Reference Rs1064793101(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DNM2
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.10904473C>T
CLNSRC
CLNACC RCV000485589.1,