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 16:22205217 (forward strand) | View in location tab

Most severe consequence
HGVS name

16:g.22205217C>T

About this variant

This variant overlaps 2 transcripts.

Variation displays