RGD:11609808 Rat Genome Database

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Variant: RGD:11609808 -  Homo sapiens

RGD ID: 11609808
RS ID: rs73411798
ClinVar ID: CV318255
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 9 14,737,005
GRCh38 9 14,737,007
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_017005.2:g.178230T>C
NC_000009.12:g.14737007A>G
NC_000009.11:g.14737005A>G
NM_001370061.1:c.*389T>C
More...
01/13/2018 3 prime utr variant benign|uncertain significance Manitoba Trichoanal syndrome; Marles Greenberg Persaud syndrome; Marles syndrome; Unilateral upper eyelid coloboma, aberrant anterior hairline pattern, and anal anomalies
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000373224 CLINVAR
dbSNP (RS) rs73411798 CLINVAR
MedGen C1855425 CLINVAR
NCBI Gene FREM1 CLINVAR
OMIM 248450 CLINVAR
  608944 CLINVAR