RGD:405132660 Rat Genome Database

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Variant: RGD:405132660 -  Homo sapiens

RGD ID: 405132660
ClinVar ID: CV2901725
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC12A3  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 16 56,911,978
GRCh38 16 56,878,066
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001126107.2:c.1093-11C>G
NM_001410896.1:c.1093-11C>G
NM_000339.3:c.1096-11C>G
NM_001126108.2:c.1096-11C>G
More... 		08/14/2023 intron variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003560173 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC12A3 CLINVAR
OMIM 600968 CLINVAR