RGD:8643937 Rat Genome Database

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Variant: RGD:8643937 -  Homo sapiens

RGD ID: 8643937
RS ID: rs61748132
ClinVar ID: CV103279
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SRD5A2  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 31,805,971
GRCh38 2 31,580,902
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008365.1:g.5070C>A
NC_000002.12:g.31580902G>T
NC_000002.11:g.31805971G>T
NM_000348.4:c.-2C>A
More... 		5 prime utr variant|utr-5 not provided none provided

Variant Details
Variant Transcripts
Gene Symbol:SRD5A2
Accession:NM_000348
Location:5UTRS;EXON

Gene Symbol:SRD5A2
Accession:XM_011533069
Location:INTRON

Gene Symbol:SRD5A2
Accession:XM_011533072
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000083636 CLINVAR
dbSNP (RS) rs61748132 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene SRD5A2 CLINVAR
OMIM 607306 CLINVAR