rs41308828 Rat Genome Database

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Variant: rs41308828 -  Homo sapiens

RGD ID: 150332967
RS ID: rs41308828
ClinVar ID: CV1168890
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ALS2  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 202,614,632
GRCh38 2 201,749,909
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_654t1:c.1738-120A>C
NM_020919.4:c.1738-120A>C
NC_000002.11:g.202614632T>G
NC_000002.12:g.201749909T>G
More... 		07/03/2018 intron variant benign none provided

Gene Symbol:ALS2
Accession:XM_017004572
Location:INTRON

Gene Symbol:ALS2
Accession:XM_047445238
Location:INTRON

Gene Symbol:ALS2
Accession:NM_001410975
Location:INTRON

Gene Symbol:ALS2
Accession:NM_020919
Location:INTRON

Gene Symbol:ALS2
Accession:XM_006712655
Location:INTRON

Gene Symbol:ALS2
Accession:XM_017004570
Location:INTRON

Gene Symbol:ALS2
Accession:XM_047445224
Location:INTRON

Gene Symbol:ALS2
Accession:XM_006712654
Location:INTRON

Gene Symbol:ALS2
Accession:NM_001135745
Location:INTRON

Gene Symbol:ALS2
Accession:XM_047445241
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001537097 CLINVAR
dbSNP (RS) rs41308828 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ALS2 CLINVAR
OMIM 606352 CLINVAR