RGD:25328206 Rat Genome Database

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Variant: RGD:25328206 -  Homo sapiens

RGD ID: 25328206
RS ID: rs1575373280
ClinVar ID: CV815280
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 37,034,804
GRCh38 3 36,993,313
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
LRG_216t1:c.-235T>A
LRG_216:g.4964T>A
NG_007109.2:g.4964T>A
NG_008418.1:g.4992A>T
More... 		12/05/2018 uncertain significance Cancer predisposition; Hereditary Cancer Syndrome; Hereditary neoplastic syndrome; Neoplastic Syndromes, Hereditary; Tumor predisposition
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001015288 CLINVAR
dbSNP (RS) rs1575373280 CLINVAR
MedGen C0027672 CLINVAR
NCBI Gene MLH1 CLINVAR
OMIM 120436 CLINVAR
SNOMED CT 699346009 CLINVAR