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rs760270633

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs760270633(C;T)
Make rs760270633(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position128220201
GeneDNM1
is asnp
is mentioned by
dbSNPrs760270633
dbSNP (classic)rs760270633
ClinGenrs760270633
ebirs760270633
HLIrs760270633
Exacrs760270633
Gnomadrs760270633
Varsomers760270633
LitVarrs760270633
Maprs760270633
PheGenIrs760270633
Biobankrs760270633
1000 genomesrs760270633
hgdprs760270633
ensemblrs760270633
geneviewrs760270633
scholarrs760270633
googlers760270633
pharmgkbrs760270633
gwascentralrs760270633
openSNPrs760270633
23andMers760270633
SNPshotrs760270633
SNPdbers760270633
MSV3drs760270633
GWAS Ctlgrs760270633
Max Magnitude0
ClinVar
Risk rs760270633(T;T)
Alt rs760270633(T;T)
Reference Rs760270633(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DNM1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130982480C>T
CLNSRC
CLNACC RCV000263789.1,