RGD:11609910 Rat Genome Database

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Variant: RGD:11609910 -  Homo sapiens

RGD ID: 11609910
RS ID: rs11575755
ClinVar ID: CV309527
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HABP2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 115,337,913
GRCh38 10 113,578,154
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008956.1:g.30136C>T
NC_000010.11:g.113578154C>T
NC_000010.10:g.115337913C>T
NM_004132.3:c.568+9C>T
More... 		05/26/2021 intron variant benign|likely benign Factor vii-activating protease marburg i; none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:HABP2
Accession:NM_001177660
Location:INTRON

Gene Symbol:HABP2
Accession:NM_004132
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000374086 CLINVAR
  RCV000947284 CLINVAR
dbSNP (RS) rs11575755 CLINVAR
MedGen C3661900 CLINVAR
  CN068943 CLINVAR
NCBI Gene HABP2 CLINVAR
OMIM 603924 CLINVAR