rs79812041 Rat Genome Database

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Variant: rs79812041 -  Homo sapiens

RGD ID: 150473576
RS ID: rs79812041
ClinVar ID: CV1217652
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ALS2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 2 202,587,586
GRCh38 2 201,722,863
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_654t1:c.3702+180A>G
NM_020919.4:c.3702+180A>G
LRG_654:g.63310A>G
NG_008775.1:g.63310A>G
More... 		07/27/2018 intron variant benign none provided

Gene Symbol:ALS2
Accession:NM_001410975
Location:INTRON

Gene Symbol:ALS2
Accession:XM_017004572
Location:INTRON

Gene Symbol:ALS2
Accession:XM_047445241
Location:INTRON

Gene Symbol:ALS2
Accession:XM_006712655
Location:INTRON

Gene Symbol:ALS2
Accession:XM_006712654
Location:INTRON

Gene Symbol:ALS2
Accession:XM_017004570
Location:INTRON

Gene Symbol:ALS2
Accession:NM_001135745
Location:INTRON

Gene Symbol:ALS2
Accession:XM_047445238
Location:INTRON

Gene Symbol:ALS2
Accession:NM_020919
Location:INTRON

Gene Symbol:ALS2
Accession:XM_047445224
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001615663 CLINVAR
dbSNP (RS) rs79812041 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ALS2 CLINVAR
OMIM 606352 CLINVAR