rs140103005 Rat Genome Database

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Variant: rs140103005 -  Homo sapiens

RGD ID: 150450499
RS ID: rs140103005
ClinVar ID: CV1260965
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CFHR2  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 196,913,197
GRCh38 1 196,944,067
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_1216:g.5300C>G
LRG_1216t1:c.58+129C>G
NM_001312672.1:c.58+129C>G
NM_005666.4:c.58+129C>G
More... 		06/18/2021 intron variant benign none provided

Gene Symbol:CFHR2
Accession:XM_011509459
Location:5UTRS;INTRON

Gene Symbol:CFHR2
Accession:NM_001410924
Location:INTRON

Gene Symbol:CFHR2
Accession:NM_005666
Location:INTRON

Gene Symbol:CFHR2
Accession:XM_011509460
Location:INTRON

Gene Symbol:CFHR2
Accession:XM_011509458
Location:INTRON

Gene Symbol:CFHR2
Accession:NM_001312672
Location:INTRON

Gene Symbol:CFHR2
Accession:XM_017001109
Location:INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001680634 CLINVAR
dbSNP (RS) rs140103005 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CFHR2 CLINVAR
OMIM 600889 CLINVAR