rs12198468 Rat Genome Database

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Variant: rs12198468 -  Homo sapiens

RGD ID: 150438143
RS ID: rs12198468
ClinVar ID: CV1264782
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 74,171,384
GRCh38 6 73,461,661
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Clinical Significance
Trait Synonyms
NG_032856.2:g.4931C>A
NC_000006.12:g.73461661C>A
NC_000006.11:g.74171384C>A
 06/23/2018 benign none provided

.


Database
Acc Id
Source(s)
ClinVar RCV001678775 CLINVAR
dbSNP (RS) rs12198468 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MTO1 CLINVAR
OMIM 614667 CLINVAR