Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: 0.17 (A)
Location

Chromosome 6:136999859 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs59766138, rs1744050

HGVS name

6:g.136999859A>T

About this variant

This variant overlaps 5 transcripts and has 2779 sample genotypes.

Variant displays