rs7771150 Rat Genome Database

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Variant: rs7771150 -  Homo sapiens

RGD ID: 14707717
RS ID: rs7771150
ClinVar ID: CV661063
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FIG4  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 110,038,102
GRCh38 6 109,716,899
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_007977.1:g.30679G>A
NC_000006.11:g.110038102G>A
LRG_241t1:c.289+331G>A
NM_014845.5:c.289+331G>A
More... 		06/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FIG4
Accession:NM_014845
Location:INTRON

Gene Symbol:FIG4
Accession:XM_011536281
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000826921 CLINVAR
dbSNP (RS) rs7771150 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FIG4 CLINVAR
OMIM 609390 CLINVAR