Original source

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

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

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

Co-located

with dbSNP rs540959701 (T/-)

Most severe consequence

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

About this variant

This variant overlaps 4 transcripts and has 36 individual genotypes.

Variation displays