RGD:28878571 Rat Genome Database

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Variant: RGD:28878571 -  Homo sapiens

RGD ID: 28878571
RS ID: rs371692085
ClinVar ID: CV902314
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRPM6  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 77,338,610
GRCh38 9 74,723,694
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000009.12:g.74723694C>A
NC_000009.11:g.77338610C>A
NM_017662.4:c.*919G>T
NM_001177311.2:c.*919G>T
More... 		01/13/2018 3 prime utr variant likely benign HYPOMAGNESEMIA, INTESTINAL, WITH SECONDARY HYPOCALCEMIA; HYPOMAGNESEMIC TETANY
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TRPM6
Accession:NM_017662
Location:3UTRS;EXON

Gene Symbol:TRPM6
Accession:NM_001177310
Location:3UTRS;EXON

Gene Symbol:TRPM6
Accession:NM_001177311
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001166783 CLINVAR
dbSNP (RS) rs371692085 CLINVAR
MedGen C1865974 CLINVAR
NCBI Gene TRPM6 CLINVAR
OMIM 602014 CLINVAR
  607009 CLINVAR