rs7674673 Rat Genome Database

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Variant: rs7674673 -  Homo sapiens

RGD ID: 150508490
RS ID: rs7674673
ClinVar ID: CV1284295
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PKD2  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 88,959,977
GRCh38 4 88,038,825
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000297.4:c.1094+324T>A
NG_008604.1:g.36158T>A
NC_000004.12:g.88038825T>A
NC_000004.11:g.88959977T>A
 08/23/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PKD2
Accession:XM_011532030
Location:INTRON

Gene Symbol:PKD2
Accession:XM_011532028
Location:INTRON

Gene Symbol:PKD2
Accession:NM_000297
Location:INTRON

Gene Symbol:PKD2
Accession:XM_011532029
Location:INTRON

Gene Symbol:PKD2
Accession:NR_156488
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001720403 CLINVAR
dbSNP (RS) rs7674673 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PKD2 CLINVAR
OMIM 173910 CLINVAR