rs75229850 Rat Genome Database

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Variant: rs75229850 -  Homo sapiens

RGD ID: 150407829
RS ID: rs75229850
ClinVar ID: CV1193537
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DIAPH1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 140,903,676
GRCh38 5 141,524,109
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000005.10:g.141524109C>T
NG_011594.2:g.99947G>A
LRG_1117t2:c.3661+34G>A
NC_000005.9:g.140903676C>T
More... 		07/31/2018 intron variant likely benign none provided

Gene Symbol:DIAPH1
Accession:NM_001079812
Location:INTRON

Gene Symbol:DIAPH1
Accession:NM_005219
Location:INTRON

Gene Symbol:DIAPH1
Accession:NM_001314007
Location:INTRON

Gene Symbol:DIAPH1
Accession:XM_047416885
Location:INTRON

Gene Symbol:DIAPH1
Accession:XM_047416884
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV001572451 CLINVAR
dbSNP (RS) rs75229850 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene DIAPH1 CLINVAR
OMIM 602121 CLINVAR