rs762585789 Rat Genome Database

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Variant: rs762585789 -  Homo sapiens

RGD ID: 12896556
RS ID: rs762585789
ClinVar ID: CV389417
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GJC2  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 228,345,454
GRCh38 1 228,157,753
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NG_011838.1:g.12902G>C
NC_000001.11:g.228157753G>C
NC_000001.10:g.228345454G>C
NM_020435.4:c.-6G>C
More... 		03/16/2019 5 prime utr variant benign AllHighlyPenetrant; none provided

Gene Symbol:GJC2
Accession:NM_020435
Location:5UTRS;EXON

.
PMID:24033266  



Database
Acc Id
Source(s)
ClinVar RCV000455508 CLINVAR
  RCV001653795 CLINVAR
dbSNP (RS) rs762585789 CLINVAR
MedGen CN169374 CLINVAR
  CN517202 CLINVAR
NCBI Gene GJC2 CLINVAR
OMIM 608803 CLINVAR