Original source

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

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

Chromosome 2:9605728 (forward strand) | View in location tab


with dbSNP rs540959701 (T/-)

Most severe consequence
Intron variant

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

About this variant

This variant overlaps 4 transcripts and has 36 sample genotypes.

Variant displays