Original source

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

Alleles
T/A|Ancestral: A|Ambiguity code: W|MAF: 0.01 (T)
Location

Chromosome 9:27556039 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57927358

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2687 sample genotypes.

Variant displays