RGD:8622305 Rat Genome Database

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Variant: RGD:8622305 -  Homo sapiens

RGD ID: 8622305
RS ID: rs28485918
ClinVar ID: CV77324
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 17 42,993,372
GRCh38 17 44,916,004
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000017.11:g.44916004A>T
NC_000017.10:g.42993372A>T
NM_002055.4:c.-518T>A
NG_008401.2:g.4496T>A
More... 		neargene-5|2kb upstream variant not provided none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000056819 CLINVAR
dbSNP (RS) rs28485918 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GFAP CLINVAR
OMIM 137780 CLINVAR