Original source

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

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

Chromosome 6:168059620 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs619706

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 271 sample genotypes.

Variant displays