Original source

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

GTT/- | MAF: 0.11 (-)

Chromosome 15:40722530-40722532 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs374610247

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2504 sample genotypes.

Variant displays