RGD:11646159 Rat Genome Database

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Variant: RGD:11646159 -  Homo sapiens

RGD ID: 11646159
RS ID: rs886063754
ClinVar ID: CV317705
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 14,735,622
GRCh38 9 14,735,624
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.179613C>T
NC_000009.12:g.14735624G>A
NC_000009.11:g.14735622G>A
NR_163238.1:n.7702C>T
More... 		01/13/2018 3 prime utr variant 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 RCV000269458 CLINVAR
dbSNP (RS) rs886063754 CLINVAR
MedGen C1855425 CLINVAR
NCBI Gene FREM1 CLINVAR
OMIM 248450 CLINVAR
  608944 CLINVAR