Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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