Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

A/G | Ancestral: A | Ambiguity code: R

Chromosome 3:41232446 (forward strand) | View in location tab

Most severe consequence
Intron variant
HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 259 sample genotypes.

Variant displays