Original source

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

T/C | Ancestral: T | Ambiguity code: Y

Chromosome 11:44226846 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs406999

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 272 sample genotypes.

Variant displays