rs34984157 Rat Genome Database

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Variant: rs34984157 -  Homo sapiens

RGD ID: 150480815
RS ID: rs34984157
ClinVar ID: CV1258798
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: SLC41A2  
Reference Nucleotide: A
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 12 105,260,367
GRCh38 12 104,866,589
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001352169.2:c.1028-9del
NM_001352170.3:c.1028-9del
NM_001352171.3:c.1028-9del
NM_001352172.3:c.1028-9del
More... 		05/04/2021 intron variant benign none provided

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Database
Acc Id
Source(s)
ClinVar RCV001685928 CLINVAR
dbSNP (RS) rs34984157 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC41A2 CLINVAR
OMIM 610802 CLINVAR