Original source

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

A/T | Ancestral: A | Ambiguity code: W | MAF: 0.49 (T)

Chromosome 8:93921193 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57145338

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 2567 sample genotypes.

Variant displays