rs9506430 Rat Genome Database

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Variant: rs9506430 -  Homo sapiens

RGD ID: 150478645
RS ID: rs9506430
ClinVar ID: CV1238941
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GJA3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 13 20,717,743
GRCh38 13 20,143,604
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_021954.4:c.-17-299G>A
NG_016399.1:g.22441G>A
NC_000013.11:g.20143604C>T
NC_000013.10:g.20717743C>T
 07/21/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GJA3
Accession:NM_021954
Location:5UTRS;INTRON

Gene Symbol:GJA3
Accession:XM_011535048
Location:5UTRS;INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001652406 CLINVAR
dbSNP (RS) rs9506430 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GJA3 CLINVAR
OMIM 121015 CLINVAR