rs12727781 Rat Genome Database

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Variant: rs12727781 -  Homo sapiens

RGD ID: 150448196
RS ID: rs12727781
ClinVar ID: CV1261935
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CFHR2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 196,927,788
GRCh38 1 196,958,658
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1216:g.19891A>G
NG_042816.1:g.19891A>G
NC_000001.11:g.196958658A>G
NC_000001.10:g.196927788A>G
More... 		11/10/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CFHR2
Accession:NM_005666
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:CFHR2
Accession:XM_011509459
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

Gene Symbol:CFHR2
Accession:NM_001410924
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001680320 CLINVAR
dbSNP (RS) rs12727781 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CFHR2 CLINVAR
OMIM 600889 CLINVAR