Original source

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

A/T | Ancestral: A | Ambiguity code: W

Chromosome 11:44226718 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs416822

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 266 sample genotypes.

Variant displays