rs2903248 Rat Genome Database

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Variant: rs2903248 -  Homo sapiens

RGD ID: 150449263
RS ID: rs2903248
ClinVar ID: CV1215084
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: C19orf12  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 19 30,196,432
GRCh38 19 29,705,525
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001282931.3:c.-153-131A>C
NM_001282929.1:c.-32-2548A>C
NM_001282930.3:c.-32-2548A>C
NM_001031726.4:c.161-2548A>C
More... 		04/16/2019 intron variant benign none provided

Gene Symbol:C19orf12
Accession:XM_047439497
Location:5UTRS;EXON

Gene Symbol:C19orf12
Accession:NM_001282929
Location:5UTRS;INTRON

Gene Symbol:C19orf12
Accession:NM_001282931
Location:5UTRS;INTRON

Gene Symbol:C19orf12
Accession:NM_001282930
Location:5UTRS;INTRON

Gene Symbol:C19orf12
Accession:NM_001256046
Location:INTRON

Gene Symbol:C19orf12
Accession:XM_047439496
Location:INTRON

Gene Symbol:C19orf12
Accession:XM_024451735
Location:INTRON

Gene Symbol:C19orf12
Accession:XM_024451734
Location:INTRON

Gene Symbol:C19orf12
Accession:NM_031448
Location:INTRON

Gene Symbol:C19orf12
Accession:NM_001256047
Location:INTRON

Gene Symbol:C19orf12
Accession:NM_001031726
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV001611674 CLINVAR
dbSNP (RS) rs2903248 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene C19orf12 CLINVAR
OMIM 614297 CLINVAR