RGD:11603727 Rat Genome Database

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Variant: RGD:11603727 -  Homo sapiens

RGD ID: 11603727
RS ID: rs183472001
ClinVar ID: CV315466
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GDF6  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 97,154,669
GRCh38 8 96,142,441
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001001557.4:c.*2122C>T
NG_008981.1:g.23352C>T
NC_000008.11:g.96142441G>A
NC_000008.10:g.97154669G>A
More... 		01/12/2018 3 prime utr variant benign|likely benign CERVICAL VERTEBRAL FUSION, AUTOSOMAL DOMINANT
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:GDF6
Accession:NM_001001557
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000302702 CLINVAR
dbSNP (RS) rs183472001 CLINVAR
MedGen C1861689 CLINVAR
NCBI Gene GDF6 CLINVAR
OMIM 118100 CLINVAR
  601147 CLINVAR