rs3802376 Rat Genome Database

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Variant: rs3802376 -  Homo sapiens

RGD ID: 150410195
RS ID: rs3802376
ClinVar ID: CV1190998
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ROR2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 9 94,518,604
GRCh38 9 91,756,322
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000009.12:g.91756322T>C
NC_000009.11:g.94518604T>C
NM_001318204.2:c.464-221A>G
NM_004560.4:c.464-221A>G
More... 		10/16/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ROR2
Accession:NM_004560
Location:INTRON

Gene Symbol:ROR2
Accession:XM_047423436
Location:INTRON

Gene Symbol:ROR2
Accession:XM_005252009
Location:INTRON

Gene Symbol:ROR2
Accession:XM_005252008
Location:INTRON

Gene Symbol:ROR2
Accession:XM_006717121
Location:INTRON

Gene Symbol:ROR2
Accession:XM_047423435
Location:INTRON

Gene Symbol:ROR2
Accession:XM_047423437
Location:INTRON

Gene Symbol:ROR2
Accession:XM_017014762
Location:INTRON

Gene Symbol:ROR2
Accession:XM_047423434
Location:INTRON

Gene Symbol:ROR2
Accession:NM_001318204
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001565923 CLINVAR
dbSNP (RS) rs3802376 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ROR2 CLINVAR
OMIM 602337 CLINVAR