rs34322451 Rat Genome Database

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Variant: rs34322451 -  Homo sapiens

RGD ID: 150463048
RS ID: rs34322451
ClinVar ID: CV1214731
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 10,419,964
GRCh38 6 10,419,731
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Clinical Significance
Trait Synonyms
NC_000006.11:g.10419964C>A
NG_016151.1:g.4834G>T
NC_000006.12:g.10419731C>A
 06/28/2018 benign none provided

.


Database
Acc Id
Source(s)
ClinVar RCV001613724 CLINVAR
dbSNP (RS) rs34322451 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TFAP2A CLINVAR
OMIM 107580 CLINVAR