Original source

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

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

Chromosome 11:2162628 (forward strand) | View in location tab

Most severe consequence
HGVS name

11:g.2162628C>T

About this variant

This variant overlaps 21 transcripts.

Variation displays