RGD:597775197 Rat Genome Database

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Variant: RGD:597775197 -  Homo sapiens

RGD ID: 597775197
ClinVar ID: CV3686645
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ILK  LOC130005201  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 6,625,546
GRCh38 11 6,604,316
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_444t1:c.45C>G
NM_001278442.2:c.-192C>G
NM_001014794.3:c.45C>G
NM_001014795.3:c.45C>G
More... 		10/24/2024 5 prime utr variant likely benign AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004929323 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene ILK CLINVAR
  LOC130005201 CLINVAR
OMIM 602366 CLINVAR