RGD:28880876 Rat Genome Database

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Variant: RGD:28880876 -  Homo sapiens

RGD ID: 28880876
RS ID: rs553601772
ClinVar ID: CV901610
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 14,736,742
GRCh38 9 14,736,744
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000009.11:g.14736742T>A
NG_017005.2:g.178493A>T
NC_000009.12:g.14736744T>A
NR_163239.1:n.8000A>T
More... 		01/13/2018 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 RCV001167467 CLINVAR
dbSNP (RS) rs553601772 CLINVAR
MedGen C1855425 CLINVAR
NCBI Gene FREM1 CLINVAR
OMIM 248450 CLINVAR
  608944 CLINVAR