rs61821986 Rat Genome Database

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Variant: rs61821986 -  Homo sapiens

RGD ID: 150497862
RS ID: rs61821986
ClinVar ID: CV1256780
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 160,001,969
GRCh38 1 160,032,179
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NG_012238.1:g.4815G>A
NC_000001.11:g.160032179C>T
NC_000001.10:g.160001969C>T
 02/13/2020 benign none provided

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001676272 CLINVAR
dbSNP (RS) rs61821986 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PIGM CLINVAR
OMIM 610273 CLINVAR