rs76943968 Rat Genome Database

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Variant: rs76943968 -  Homo sapiens

RGD ID: 14723923
RS ID: rs76943968
ClinVar ID: CV661909
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MTO1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 74,175,894
GRCh38 6 73,466,171
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001123226.2:c.218-38G>A
NM_012123.4:c.218-38G>A
NM_133645.3:c.218-38G>A
NG_032856.2:g.9441G>A
More... 		06/14/2018 intron variant likely benign none provided

Gene Symbol:MTO1
Accession:NM_133645
Location:INTRON

Gene Symbol:MTO1
Accession:NM_001123226
Location:INTRON

Gene Symbol:MTO1
Accession:NM_012123
Location:INTRON

Gene Symbol:MTO1
Accession:XM_047418605
Location:INTRON

Gene Symbol:MTO1
Accession:XM_047418606
Location:INTRON

Gene Symbol:MTO1
Accession:XM_047418607
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV000832753 CLINVAR
dbSNP (RS) rs76943968 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MTO1 CLINVAR
OMIM 614667 CLINVAR