RGD:150498396 Rat Genome Database

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Variant: RGD:150498396 -  Homo sapiens

RGD ID: 150498396
RS ID: rs41274346
ClinVar ID: CV1255572
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 17,565,981
GRCh38 11 17,544,434
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_033191.2:g.2062G>A
NG_011883.2:g.4983C>T
NC_000011.10:g.17544434G>A
NC_000011.9:g.17565981G>A
 06/29/2018 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001676360 CLINVAR
dbSNP (RS) rs41274346 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene USH1C CLINVAR
OMIM 605242 CLINVAR