RGD:28880882 Rat Genome Database

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Variant: RGD:28880882 -  Homo sapiens

RGD ID: 28880882
RS ID: rs73411795
ClinVar ID: CV901611
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 14,736,778
GRCh38 9 14,736,780
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NC_000009.12:g.14736780C>T
NC_000009.11:g.14736778C>T
NG_017005.2:g.178457G>A
NM_001177704.2:c.*616G>A
More... 		01/13/2018 likely benign 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 RCV001167468 CLINVAR
dbSNP (RS) rs73411795 CLINVAR
MedGen C1855425 CLINVAR
NCBI Gene FREM1 CLINVAR
OMIM 248450 CLINVAR
  608944 CLINVAR