Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

A/G | Ancestral: G | Ambiguity code: R

Chromosome 7:76437883 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs1799219

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays