RGD:11657033 Rat Genome Database

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Variant: RGD:11657033 -  Homo sapiens

RGD ID: 11657033
RS ID: rs199614038
ClinVar ID: CV290362
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 51,259,460
GRCh38 2 51,032,322
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_011878.1:g.5215G>C
NC_000002.12:g.51032322C>G
NC_000002.11:g.51259460C>G
NM_001135659.1:c.-1263G>C
More... 		01/12/2018 5 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000338021 CLINVAR
dbSNP (RS) rs199614038 CLINVAR
MedGen C3280479 CLINVAR
NCBI Gene NRXN1 CLINVAR
OMIM 600565 CLINVAR
  614325 CLINVAR