Original source

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

Alleles
G/- | Ancestral: T
Location

Chromosome 10:119662226 (forward strand) | View in location tab

Co-located

with dbSNP rs2736423 (G/T)

Most severe consequence

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts.

Variation displays