Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

C/A | Ancestral: A | Ambiguity code: M

Chromosome 12:6840746 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant

Archive dbSNP rs386503888

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 21 transcripts and has 1 sample genotype.

Variant displays