Original source

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

GAAT/- | MAF: 0.02 (-)

Chromosome 19:45421041-45421044 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs148140947, rs34119263

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 15 transcripts and has 2591 sample genotypes.

Variant displays