Most severe consequence
38
Intergenic variant
Alleles
C/G
Location
Contig ADFV01162226.1:2148 (forward strand)|View in location tab
HGVS name
ADFV01162226.1:g.2148C>G
Synonyms
ENSEMBL ENSNLESNP1
Original source
Variants (including SNPs and indels) imported from dbSNP [mapped to the assembly Nleu1.0] (release 145)|View in dbSNP
About this variant
This variant has 1 sample genotype.
