rs6964163 Rat Genome Database

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Variant: rs6964163 -  Homo sapiens

RGD ID: 150485917
RS ID: rs6964163
ClinVar ID: CV1280868
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SRI  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 87,840,263
GRCh38 7 88,210,948
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001256892.2:c.161-23A>G
NM_198901.2:c.161-23A>G
NM_001256891.2:c.206-23A>G
NM_003130.4:c.206-23A>G
More... 		05/16/2021 intron variant benign none provided

Gene Symbol:SRI
Accession:NM_198901
Location:INTRON

Gene Symbol:SRI
Accession:NM_003130
Location:INTRON

Gene Symbol:SRI
Accession:NM_001256892
Location:INTRON

Gene Symbol:SRI
Accession:NM_001256891
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001715694 CLINVAR
dbSNP (RS) rs6964163 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SRI CLINVAR
OMIM 182520 CLINVAR