Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.28 (A)

Chromosome 13:75589660 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17064748, rs12877452

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2700 sample genotypes.

Variant displays