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rs1057523007

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523007(C;C)
Make rs1057523007(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position32679458
GeneDNM1L
is asnp
is mentioned by
dbSNPrs1057523007
dbSNP (old)rs1057523007
ClinGenrs1057523007
ebirs1057523007
HLIrs1057523007
Exacrs1057523007
Gnomadrs1057523007
Varsomers1057523007
LitVarrs1057523007
Maprs1057523007
PheGenIrs1057523007
Biobankrs1057523007
1000 genomesrs1057523007
hgdprs1057523007
ensemblrs1057523007
gopubmedrs1057523007
geneviewrs1057523007
scholarrs1057523007
googlers1057523007
pharmgkbrs1057523007
gwascentralrs1057523007
openSNPrs1057523007
23andMers1057523007
23andMe allrs1057523007
SNPshotrs1057523007
SNPdbers1057523007
MSV3drs1057523007
GWAS Ctlgrs1057523007
Max Magnitude0
ClinVar
Risk rs1057523007(C;C)
Alt rs1057523007(C;C)
Reference Rs1057523007(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DNM1L
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.32832392G>C
CLNSRC
CLNACC RCV000439994.1,