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rs754404446

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs754404446(A;A)
Make rs754404446(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position128242281
GeneDNM1
is asnp
is mentioned by
dbSNPrs754404446
dbSNP (classic)rs754404446
ClinGenrs754404446
ebirs754404446
HLIrs754404446
Exacrs754404446
Gnomadrs754404446
Varsomers754404446
LitVarrs754404446
Maprs754404446
PheGenIrs754404446
Biobankrs754404446
1000 genomesrs754404446
hgdprs754404446
ensemblrs754404446
geneviewrs754404446
scholarrs754404446
googlers754404446
pharmgkbrs754404446
gwascentralrs754404446
openSNPrs754404446
23andMers754404446
SNPshotrs754404446
SNPdbers754404446
MSV3drs754404446
GWAS Ctlgrs754404446
Max Magnitude0
ClinVar
Risk rs754404446(A;A) rs754404446(C;C)
Alt rs754404446(A;A) rs754404446(C;C)
Reference Rs754404446(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DNM1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.131004560G>A
CLNSRC
CLNACC RCV000413377.1,