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rs1057523861

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523861(A;A)
Make rs1057523861(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position32710995
GeneDNM1L
is asnp
is mentioned by
dbSNPrs1057523861
dbSNP (classic)rs1057523861
ClinGenrs1057523861
ebirs1057523861
HLIrs1057523861
Exacrs1057523861
Gnomadrs1057523861
Varsomers1057523861
LitVarrs1057523861
Maprs1057523861
PheGenIrs1057523861
Biobankrs1057523861
1000 genomesrs1057523861
hgdprs1057523861
ensemblrs1057523861
geneviewrs1057523861
scholarrs1057523861
googlers1057523861
pharmgkbrs1057523861
gwascentralrs1057523861
openSNPrs1057523861
23andMers1057523861
23andMe allrs1057523861
SNPshotrs1057523861
SNPdbers1057523861
MSV3drs1057523861
GWAS Ctlgrs1057523861
Max Magnitude0
ClinVar
Risk rs1057523861(A;A)
Alt rs1057523861(A;A)
Reference Rs1057523861(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DNM1L
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.32863929G>A
CLNSRC
CLNACC RCV000443148.1,